fda-device · Food and Drug Administration · Rule · Published 2020-04-02 · Effective 2020-04-01 · 85 FR 18439
Document
Document number
2020-06354
Federal Register citation
85 FR 18439
CFR reference
21 CFR 5
Type
Rule
Action
Final rule; technical amendments.
Category
fda-device
Sub-agency
Food and Drug Administration
Publication date
2020-04-02
Effective date
2020-04-01
HHS docket
Docket No. FDA-2020-N-0011
Abstract
The Food and Drug Administration (FDA, the Agency, or we) is amending its medical device regulations. These revisions are necessary to reflect changes to the Agency's Center for Devices and Radiological Health's organizational structure, including the reorganization of its offices. The revisions replace references to the obsolete offices and positions with the current information, update the physical addresses for such offices, and correct inaccurate citations. In addition, as part of this effort we made other editorial non-substantive changes to correct other addresses, references, and citations, as appropriate. The rule does not impose any new regulatory requirements on affected parties. This action is editorial in nature and is intended to improve the accuracy of the Agency's regulations.