Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

HGM ENDOCOAGULATOR MODEL 20

K-Number: K852913 · 1985-09-05

ApplicantHgm, Inc.
Decision Date1985-09-05
Product Code
DecisionSubstantially Equivalent

Device Summary

HGM ENDOCOAGULATOR MODEL 20 is the device name listed in this FDA 510(k) record. The listed applicant is Hgm, Inc.. It received FDA 510(k) clearance on 1985-09-05 under 510(k) number K852913. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HGM ENDOCOAGULATOR MODEL 20?

HGM ENDOCOAGULATOR MODEL 20 is a medical device that received FDA 510(k) clearance on 1985-09-05. The listed applicant is Hgm, Inc.. The 510(k) number is K852913.

When did HGM ENDOCOAGULATOR MODEL 20 receive FDA 510(k) clearance?

HGM ENDOCOAGULATOR MODEL 20 received FDA 510(k) clearance on 1985-09-05, under 510(k) number K852913.

Who is the listed applicant for HGM ENDOCOAGULATOR MODEL 20?

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

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

↑