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Regulations last checked for updates: May 14, 2025
Title 21 - Food and Drugs last revised: May 12, 2025
All Titles
Title 21
Chapter I
Part 820
Subpart M - Subpart M—Records
§ 820.180 - General requirements.
§ 820.181 - Device master record.
§ 820.184 - Device history record.
§ 820.186 - Quality system record.
§ 820.198 - Complaint files.
authority:
21 U.S.C. 351
,
352
,
360
,
360
c,
360
d,
360
e,
360
h,
360
i,
360
j,
360
l,
371
,
374
,
381
,
383
;
42 U.S.C. 216
,
262
,
263a
,
264
source:
61 FR 52654, Oct. 7, 1996, unless otherwise noted.
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