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FDA 510(k)

HCG, INC. MEDICAL LASER ENDOCOAGULATOR MODEL P.C.

K-Number: K852464 · 1985-07-25

ApplicantHcg, Inc.
Decision Date1985-07-25
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

HCG, INC. MEDICAL LASER ENDOCOAGULATOR MODEL P.C. is the device name listed in this FDA 510(k) record. The listed applicant is Hcg, Inc.. It received FDA 510(k) clearance on 1985-07-25 under 510(k) number K852464. 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 HCG, INC. MEDICAL LASER ENDOCOAGULATOR MODEL P.C.?

HCG, INC. MEDICAL LASER ENDOCOAGULATOR MODEL P.C. is a medical device that received FDA 510(k) clearance on 1985-07-25. The listed applicant is Hcg, Inc.. The 510(k) number is K852464.

When did HCG, INC. MEDICAL LASER ENDOCOAGULATOR MODEL P.C. receive FDA 510(k) clearance?

HCG, INC. MEDICAL LASER ENDOCOAGULATOR MODEL P.C. received FDA 510(k) clearance on 1985-07-25, under 510(k) number K852464.

Who is the listed applicant for HCG, INC. MEDICAL LASER ENDOCOAGULATOR MODEL P.C.?

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

What is the FDA product code for HCG, INC. MEDICAL LASER ENDOCOAGULATOR MODEL P.C.?

The FDA product code for HCG, INC. MEDICAL LASER ENDOCOAGULATOR MODEL P.C. 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.

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