HHS - 21 CFR PART 607
ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS AND LICENSED DEVICES
active, Most Current
| Organization: | HHS |
| Publication Date: | 1 April 2020 |
| Status: | active |
| Page Count: | 7 |
scope:
(a) This part establishes establishment registration and product listing requirements for manufacturers of human blood and blood products.
(b) This part establishes establishment registration and product listing requirements for manufacturers of products that meet the definition of a device under the Federal Food, Drug, and Cosmetic Act and that are licensed under section 351 of the Public Health Service Act, as well as licensed biological products used in the manufacture of a licensed device.
[81 FR 60221, Aug. 31, 2016]
Document History
April 1, 2023
ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS AND LICENSED DEVICES
(a) This part establishes establishment registration and product listing requirements for manufacturers of human blood and blood products.
(b) This part establishes establishment registration and...
April 1, 2022
ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS AND LICENSED DEVICES
(a) This part establishes establishment registration and product listing requirements for manufacturers of human blood and blood products.
(b) This part establishes establishment registration and...
April 1, 2021
ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS AND LICENSED DEVICES
(a) This part establishes establishment registration and product listing requirements for manufacturers of human blood and blood products.
(b) This part establishes establishment registration and...
21 CFR PART 607
April 1, 2020
ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS AND LICENSED DEVICES
(a) This part establishes establishment registration and product listing requirements for manufacturers of human blood and blood products.
(b) This part establishes establishment registration and...
April 1, 2019
ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS AND LICENSED DEVICES
(a) This part establishes establishment registration and product listing requirements for manufacturers of human blood and blood products.
(b) This part establishes establishment registration and...
April 1, 2018
ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS
This part establishes establishment registration and product listing requirements for manufacturers of human blood and blood products.
This part establishes establishment registration and product...
April 1, 2017
ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS
(a) This part establishes establishment registration and product listing requirements for manufacturers of human blood and blood products.
(b) This part establishes establishment registration and...
April 1, 2016
ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS
A description is not available for this item.
April 1, 2015
ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS
A description is not available for this item.
April 1, 2014
ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS
A description is not available for this item.