# Medical Devices; Exemptions From Premarket Notification for Certain Classified Devices; Correction
> **Food and Drug Administration** · Final rule; correction. · Published 1995-03-28 · Effective 1995-01-06 · 60 FR 15872
## Document
- **Document number:** 95-7512
- **Category:** fda-device
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 60 FR 15872
- **CFR reference:** 21 CFR 886
- **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.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/1995/03/28/95-7512/medical-devices-exemptions-from-premarket-notification-for-certain-classified-devices-correction)
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