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HHS - 21 CFR PART 809

IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE

active, Most Current
Organization: HHS
Publication Date: 1 April 2022
Status: active
Page Count: 10

Document History

21 CFR PART 809
April 1, 2023
IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE
A description is not available for this item.
21 CFR PART 809
April 1, 2022
IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE
A description is not available for this item.
21 CFR PART 809
April 1, 2021
IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE
A description is not available for this item.
21 CFR PART 809
April 1, 2020
IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE
A description is not available for this item.
21 CFR PART 809
April 1, 2019
IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE
A description is not available for this item.
21 CFR PART 809
April 1, 2018
IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE
Definitions. In vitro diagnostic products are those reagents, instruments, and systems intended for use in the diagnosis of disease or other conditions, including a determination of the state of...
21 CFR PART 809
April 1, 2017
IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE
Definitions. (a) In vitro diagnostic products are those reagents, instruments, and systems intended for use in the diagnosis of disease or other conditions, including a determination of the state of...
21 CFR PART 809
April 1, 2016
IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE
Definitions. (a) In vitro diagnostic products are those reagents, instruments, and systems intended for use in the diagnosis of disease or other conditions, including a determination of the state of...
21 CFR PART 809
April 1, 2015
IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE
A description is not available for this item.
21 CFR PART 809
April 1, 2014
IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE
Definitions. (a) In vitro diagnostic products are those reagents, instruments, and systems intended for use in the diagnosis of disease or other conditions, including a determination of the state of...
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References

This document is referenced by:
AAMI 60601-1-2 - MEDICAL ELECTRICAL EQUIPMENT – Part 1-2: General requirements for basic safety and essential performance – Collateral Standard: Electromagnetic disturbances – Requirements and tests
Published by AAMI on January 1, 2014
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of MEDICAL ELECTRICAL EQUIPMENT and MEDICAL ELECTRICAL SYSTEMS, hereafter referred to as ME EQUIPMENT and ME SYSTEMS....
This document is referenced by:
NFPA 30 - Flammable and Combustible Liquids Code
Published by NFPA on January 1, 2021
This code shall apply to the storage, handling, and use of ignitible (flammable or combustible) liquids, including waste liquids, as herein defined and classified. This code shall not apply to the...
This document is referenced by:
MM01 - Molecular Testing for Heritable Genetics and Specimen Identification
Published by CLSI on June 1, 2023
This guideline has been revised by experienced molecular laboratory professionals to focus on germline genetic diagnostic testing. It provides information for laboratories implementing molecular...
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