Cleared Traditional

K851651 - HGM ENDOCOAGULATOR MODEL 8 (FDA 510(k) Clearance)

K851651 · Hgm, Inc. · General & Plastic Surgery device
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Jul 1985
Decision
92d
Days
-
Risk

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 after a review of 92 days - within the typical 510(k) review window.

This device falls under the General & Plastic Surgery FDA review panel. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General & Plastic Surgery review framework, consistent with the majority of Class II 510(k) submissions.

View all Hgm, Inc. devices

Submission Details

510(k) Number K851651 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (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 -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
22d faster than avg
Panel avg: 114d · This submission: 92d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code -
Device Class -