HHS - 21 CFR PART 3
PRODUCT JURISDICTION
active, Most Current
Organization: | HHS |
Publication Date: | 1 April 2020 |
Status: | active |
Page Count: | 6 |
scope:
This section applies to:
(a) Any combination product, or
(b) Any product where the agency component with primary jurisdiction is unclear or in dispute.
Document History
April 1, 2023
PRODUCT JURISDICTION
Purpose.
This regulation relates to agency management and organization and has two purposes. The first is to implement section 503(g) of the act, as added by section 16 of the Safe Medical Devices...
April 1, 2022
PRODUCT JURISDICTION
This section applies to:
(a) Any combination product, or
(b) Any product where the agency component with primary jurisdiction is unclear or in dispute.
April 1, 2021
PRODUCT JURISDICTION
This section applies to:
(a) Any combination product, or
(b) Any product where the agency component with primary jurisdiction is unclear or in dispute.
21 CFR PART 3
April 1, 2020
PRODUCT JURISDICTION
This section applies to:
(a) Any combination product, or
(b) Any product where the agency component with primary jurisdiction is unclear or in dispute.
April 1, 2019
PRODUCT JURISDICTION
This section applies to:
(a) Any combination product, or
(b) Any product where the agency component with primary jurisdiction is unclear or in dispute.
April 1, 2018
PRODUCT JURISDICTION
This section applies to: (a) Any combination product, or (b) Any product where the agency component with primary jurisdiction is unclear or in dispute.
April 1, 2017
PRODUCT JURISDICTION
Purpose.
This regulation relates to agency management and organization and has two purposes. The first is to implement section 503(g) of the act, as added by section 16 of the Safe Medical Devices...
April 1, 2016
PRODUCT JURISDICTION
Purpose.
This regulation relates to agency management and organization and has two purposes. The first is to implement section 503(g) of the act, as added by section 16 of the Safe Medical Devices...
April 1, 2014
PRODUCT JURISDICTION
Purpose.
This regulation relates to agency management and organization and has two purposes. The first is to implement section 503(g) of the act, as added by section 16 of the Safe Medical Devices...