K851651Substantially Equivalent

Hgm Endocoagulator Model 8

Name: K851651 Hgm Endocoagulator Model 8
Creator: Hgm, Inc.
Published: 1985-07-23
License: https://open.fda.gov/license/

Hgm, Inc., Salt Lake City UT / Traditional, Substantially Equivalent

FDA source

K851651 is the FDA 510(k) clearance record for HGM ENDOCOAGULATOR MODEL 8, cleared for Hgm, Inc. on 1985-07-23. FDA records list 21 510(k) clearances for Hgm, Inc., from 1983-01-03 to 1995-08-11. As of 2026-09-10, FDA records show no recalls naming K851651.

Clearance record

Decision date: 1985-07-23
Received: 1985-04-22 (92 days to decision)
Review panel: Unknown
Applicant: Hgm, Inc. 3959 W. 1820 S., Salt Lake City UT
Third party review: No