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)

ENDOCOAGULATOR MODEL 5, 8 & 20 ARGON LASER

K-Number: K871424 · 1987-07-08

ApplicantHgm, Inc.
Decision Date1987-07-08
Product CodeLMS
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ENDOCOAGULATOR MODEL 5, 8 & 20 ARGON LASER is the device name listed in this FDA 510(k) record. The listed applicant is Hgm, Inc.. It received FDA 510(k) clearance on 1987-07-08 under 510(k) number K871424. The device is classified under product code LMS. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOCOAGULATOR MODEL 5, 8 & 20 ARGON LASER?

ENDOCOAGULATOR MODEL 5, 8 & 20 ARGON LASER is a medical device that received FDA 510(k) clearance on 1987-07-08. The listed applicant is Hgm, Inc.. The 510(k) number is K871424.

When did ENDOCOAGULATOR MODEL 5, 8 & 20 ARGON LASER receive FDA 510(k) clearance?

ENDOCOAGULATOR MODEL 5, 8 & 20 ARGON LASER received FDA 510(k) clearance on 1987-07-08, under 510(k) number K871424.

Who is the listed applicant for ENDOCOAGULATOR MODEL 5, 8 & 20 ARGON LASER?

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 ENDOCOAGULATOR MODEL 5, 8 & 20 ARGON LASER?

The FDA product code for ENDOCOAGULATOR MODEL 5, 8 & 20 ARGON LASER is LMS.

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 →

Related Devices (Code: LMS)

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.

K855146LASERSCOPE OMNIPLUS PHOTOSURGICAL SYST/ND:YAG OTOLLaserscope

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.

↑