Code of Federal Regulations, Title 21, Food and Drugs, Pt. 800-1299, Revised as

Code of Federal Regulations, Title 21, Food and Drugs, Pt. 800-1299, Revised as of April 1, 2016

Agency Publisher: National Archives and Records Administration, Office of the Federal Register
USA List Price:
$66.00 Display International Price
Availability:
In Stock
GPO Stock Number: 869-084-00074-3 ISBN: 9780160932762
Price: $66.00

Description

CFR Title 21, Parts 800-1299 rules, regulations, including labeling, medical device reporting, in vitro diagnostic products for human use, medical devices including; hematology and pathology, immunology and microbiology, anesthesiology, cardiovascular, dental, neurological, orthopedic and radiology, and, banned devise, etc., tobacco products cigarettes and smokeless tobacco, cigarette package and advertising warnings, human tissue intended for implantation, and more.

Audiences: medical device producers and marketers, medical practitioners, tobacco proudcers andmarketers, human health researchers and practioners.

Table of Contents:
800
800.10 to 800.55 GENERAL
801
801.1 to 801.437 LABELING
803
803.1 to 803.58 MEDICAL DEVICE REPORTING
806
806.1 to 806.40 MEDICAL DEVICES; REPORTS OF CORRECTIONS AND REMOVALS
807
807.3 to 807.100 ESTABLISHMENT REGISTRATION AND DEVICE LISTING FOR MANUFACTURERS AND INITIAL IMPORTERS OF DEVICES
808
808.1 to 808.101 EXEMPTIONS FROM FEDERAL PREEMPTION OF STATE AND LOCAL MEDICAL DEVICE REQUIREMENTS
809
809.3 to 809.40 IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE
810
810.1 to 810.18 MEDICAL DEVICE RECALL AUTHORITY
812
812.1 to 812.150 INVESTIGATIONAL DEVICE EXEMPTIONS
813 [RESERVED]
814
814.1 to 814.126 PREMARKET APPROVAL OF MEDICAL DEVICES
820
820.1 to 820.250 QUALITY SYSTEM REGULATION
821
821.1 to 821.60 MEDICAL DEVICE TRACKING REQUIREMENTS
822
822.1 to 822.38 POSTMARKET SURVEILLANCE
830
830.3 to 830.360 UNIQUE DEVICE IDENTIFICATION
860
860.1 to 860.136 MEDICAL DEVICE CLASSIFICATION PROCEDURES
861
861.1 to 861.38 PROCEDURES FOR PERFORMANCE STANDARDS DEVELOPMENT
862
862.1 to 862.3950 CLINICAL CHEMISTRY AND CLINICAL TOXICOLOGY DEVICES
864
864.1 to 864.9900 HEMATOLOGY AND PATHOLOGY DEVICES
866
866.1 to 866.6050 IMMUNOLOGY AND MICROBIOLOGY DEVICES
868
868.1 to 868.6885 ANESTHESIOLOGY DEVICES
870
870.1 to 870.5925 CARDIOVASCULAR DEVICES
872
872.1 to 872.6890 DENTAL DEVICES
874
874.1 to 874.5900 EAR, NOSE, AND THROAT DEVICES
876
876.1 to 876.5990 GASTROENTEROLOGY-UROLOGY DEVICES
878
878.1 to 878.5910 GENERAL AND PLASTIC SURGERY DEVICES
880
880.1 to 880.6992 GENERAL HOSPITAL AND PERSONAL USE DEVICES
882
882.1 to 882.5975 NEUROLOGICAL DEVICES
884
884.1 to 884.6200 OBSTETRICAL AND GYNECOLOGICAL DEVICES
886
886.1 to 886.5933 OPHTHALMIC DEVICES
888
888.1 to 888.5980 ORTHOPEDIC DEVICES
890
890.1 to 890.5975 PHYSICAL MEDICINE DEVICES
892
892.1 to 892.6500 RADIOLOGY DEVICES
895
895.1 to 895.101 BANNED DEVICES
898
898.11 to 898.14 PERFORMANCE STANDARD FOR ELECTRODE LEAD WIRES AND PATIENT CABLES
SUBCHAPTER I—MAMMOGRAPHY QUALITY STANDARDS ACT

900
900.1 to 900.25 MAMMOGRAPHY
SUBCHAPTER J—RADIOLOGICAL HEALTH

1000
1000.1 to 1000.60 GENERAL
1002
1002.1 to 1002.51 RECORDS AND REPORTS
1003
1003.1 to 1003.31 NOTIFICATION OF DEFECTS OR FAILURE TO COMPLY
1004
1004.1 to 1004.6 REPURCHASE, REPAIRS, OR REPLACEMENT OF ELECTRONIC PRODUCTS
1005
1005.1 to 1005.25 IMPORTATION OF ELECTRONIC PRODUCTS
1010
1010.1 to 1010.20 PERFORMANCE STANDARDS FOR ELECTRONIC PRODUCTS: GENERAL
1020
1020.10 to 1020.40 PERFORMANCE STANDARDS FOR IONIZING RADIATION EMITTING PRODUCTS
1030
1030.10 PERFORMANCE STANDARDS FOR MICROWAVE AND RADIO FREQUENCY EMITTING PRODUCTS
1040
1040.10 to 1040.30
PERFORMANCE STANDARDS FOR LIGHT-EMITTING PRODUCTS
1050
1050.10 PERFORMANCE STANDARDS FOR SONIC, INFRASONIC, AND ULTRASONIC RADIATION-EMITTING PRODUCTS
SUBCHAPTER K—TOBACCO PRODUCTS

1100
xxx
1107
1107.1 ESTABLISHMENT REGISTRATION, PRODUCT LISTING, AND SUBSTANTIAL EQUIVALENCE REPORTS
1140
1140.1 to 1140.34 CIGARETTES AND SMOKELESS TOBACCO
1141
1141.1 to 1141.16 CIGARETTE PACKAGE AND ADVERTISING WARNINGS
1143
xxx
1150
1150.1 to 1150.17 USER FEES
SUBCHAPTER L—REGULATIONS UNDER CERTAIN OTHER ACTS ADMINISTERED BY THE FOOD AND DRUG ADMINISTRATION

1210
1210.1 to 1210.31 REGULATIONS UNDER THE FEDERAL IMPORT MILK ACT
1230
1230.2 to 1230.49 REGULATIONS UNDER THE FEDERAL CAUSTIC POISON ACT
1240
1240.3 to 1240.95 CONTROL OF COMMUNICABLE DISEASES
1250
1250.3 to 1250.96 INTERSTATE CONVEYANCE SANITATION
1251-1269
[RESERVED]
1270
1270.1 to 1270.43 HUMAN TISSUE INTENDED FOR TRANSPLANTATION
1271
1271.1 to 1271.440 HUMAN CELLS, TISSUES, AND CELLULAR AND TISSUE-BASED PRODUCTS
1272-1299 [RESERVED]

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Product Details

GPO Stock Number:
869-084-00074-3
ISBN:
9780160932762
Availability Details:
In Stock - Warehouse and Retail (Priced)
USA Price:
$66.00
International Price:
$92.40
Publisher:
National Archives and Records Administration, Office of the Federal Register
Author:
 
Year/Pages:
2016: 868 p.
Note:
 
Key Phrases:
CFR Title 21
SuDocs Class:
 
Weight:
2.0625 lb.
Quantity Price:
Discount
Binding:
Paperback
Cover:
Paper
Subject Bibliography:
 
Unit of Issue (U.S.):
Each
Item Available Date:
07/27/2016
Last Status Update:
02/15/2017