HGM, INC. MEDICAL LASER ENDOCOAGULATOR MODEL 8-K
K-Number: K850572 · 1985-04-23
Advertisement
Device Summary
Frequently Asked Questions
What is the HGM, INC. MEDICAL LASER ENDOCOAGULATOR MODEL 8-K?
HGM, INC. MEDICAL LASER ENDOCOAGULATOR MODEL 8-K is a medical device that received FDA 510(k) clearance on 1985-04-23. The listed applicant is Hgm, Inc.. The 510(k) number is K850572.
When did HGM, INC. MEDICAL LASER ENDOCOAGULATOR MODEL 8-K receive FDA 510(k) clearance?
HGM, INC. MEDICAL LASER ENDOCOAGULATOR MODEL 8-K received FDA 510(k) clearance on 1985-04-23, under 510(k) number K850572.
Who is the listed applicant for HGM, INC. MEDICAL LASER ENDOCOAGULATOR MODEL 8-K?
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 HGM, INC. MEDICAL LASER ENDOCOAGULATOR MODEL 8-K?
The FDA product code for HGM, INC. MEDICAL LASER ENDOCOAGULATOR MODEL 8-K is HQF.
Related Clinical Trials
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.
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.
Related Devices (Code: HQF)
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.
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.
Advertisement