HGM ENDOCOAGULATOR MODEL 20— 510(k) K852913

Substantially Equivalent

Hgm, Inc.

FDA 510(k) clearance K852913 for HGM ENDOCOAGULATOR MODEL 20, Substantially Equivalent on 1985-09-05. Applicant: Hgm, Inc..

Clearance details

Applicant: Hgm, Inc.
Advisory panel: Unknown
Date received: 1985-07-11
Decision date: 1985-09-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

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