HGM ENDOCOAGULATOR MODEL 8— 510(k) K851651

Substantially Equivalent

Hgm, Inc.

FDA 510(k) clearance K851651 for HGM ENDOCOAGULATOR MODEL 8, Substantially Equivalent on 1985-07-23. Applicant: Hgm, Inc..

Clearance details

Applicant: Hgm, Inc.
Advisory panel: Unknown
Date received: 1985-04-22
Decision date: 1985-07-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

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