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FDA 510(k)

HGM ENDOCOAGULATOR MODEL 8

K-Number: K851651 · 1985-07-23

ApplicantHgm, Inc.
Decision Date1985-07-23
Product Code
DecisionSubstantially Equivalent

Device Summary

HGM ENDOCOAGULATOR MODEL 8 is the device name listed in this FDA 510(k) record. The listed applicant is Hgm, Inc.. It received FDA 510(k) clearance on 1985-07-23 under 510(k) number K851651. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HGM ENDOCOAGULATOR MODEL 8?

HGM ENDOCOAGULATOR MODEL 8 is a medical device that received FDA 510(k) clearance on 1985-07-23. The listed applicant is Hgm, Inc.. The 510(k) number is K851651.

When did HGM ENDOCOAGULATOR MODEL 8 receive FDA 510(k) clearance?

HGM ENDOCOAGULATOR MODEL 8 received FDA 510(k) clearance on 1985-07-23, under 510(k) number K851651.

Who is the listed applicant for HGM ENDOCOAGULATOR MODEL 8?

The FDA 510(k) record lists Hgm, Inc. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Hgm, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K950120SMART PLUGK931072HGM ILLUMINATING/ASPIRATING ENDOOCULAR PROBEK931784HGM ILLUMINATING IMAGING ENDOCULAR PROBEK933333HGM SCANMAN PLUSK931499Q-11 OPHTHALMIC LASERK925663HGM ASPIRATING ENDOOCULAR(TM) PROBE

View all 23 devices →

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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