Cleared Traditional

HGM ENDOCOAGULATOR MODEL 8

K851651 · Hgm, Inc. · General & Plastic Surgery

Jul 1985

Decision

92d

Days

—

Risk

About This 510(k) Submission

K851651 is an FDA 510(k) clearance for the HGM ENDOCOAGULATOR MODEL 8, submitted by Hgm, Inc. (Salt Lake City, US). The FDA issued a Cleared decision on July 23, 1985, 92 days after receiving the submission on April 22, 1985. This device falls under the General & Plastic Surgery review panel.

Submission Details

510(k) Number	K851651 FDA.gov
FDA Decision	Cleared SESE
Date Received	April 22, 1985
Decision Date	July 23, 1985
Days to Decision	92 days
Submission Type	Traditional
Review Panel	General & Plastic Surgery (SU)
Summary	—