FDA 510(k)

MEDICAL LASER ENDOCOAGULATOR 5K

K-Number: K840854 · 1984-04-02

Decision Date1984-04-02

Product CodeHQF

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

MEDICAL LASER ENDOCOAGULATOR 5K is the device name listed in this FDA 510(k) record. The listed applicant is Hgm, Inc.. It received FDA 510(k) clearance on 1984-04-02 under 510(k) number K840854. The device is classified under product code HQF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDICAL LASER ENDOCOAGULATOR 5K?

MEDICAL LASER ENDOCOAGULATOR 5K is a medical device that received FDA 510(k) clearance on 1984-04-02. The listed applicant is Hgm, Inc.. The 510(k) number is K840854.

When did MEDICAL LASER ENDOCOAGULATOR 5K receive FDA 510(k) clearance?

MEDICAL LASER ENDOCOAGULATOR 5K received FDA 510(k) clearance on 1984-04-02, under 510(k) number K840854.

Who is the listed applicant for MEDICAL LASER ENDOCOAGULATOR 5K?

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

What is the FDA product code for MEDICAL LASER ENDOCOAGULATOR 5K?

The FDA product code for MEDICAL LASER ENDOCOAGULATOR 5K is HQF.

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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.