Medical Devices; Exemptions From Premarket Notification for Certain Classified Devices; Correction
fda-device · Food and Drug Administration · Rule · Published 1995-03-28 · Effective 1995-01-06 · 60 FR 15872
Document
Document number
95-7512
Federal Register citation
60 FR 15872
CFR reference
21 CFR 886
Type
Rule
Action
Final rule; correction.
Category
fda-device
Sub-agency
Food and Drug Administration
Publication date
1995-03-28
Effective date
1995-01-06
HHS docket
Docket No. 94M-0260
Abstract
The Food and Drug Administration (FDA) is correcting a final rule that appeared in the Federal Register of December 7, 1994 (59 FR 63005). The document exempted 148 generic types of class I devices from the requirement of premarket notification, with limitations. The document was published with an error in the codified section. This document corrects that error. EFFECTIVE DATE: January 6, 1995.