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FDA 510(k)

ENDOCOAGULATOR MODELS 5, 8 & 20 ARGON LASER

K-Number: K870773 · 1987-07-10

ApplicantHgm, Inc.
Decision Date1987-07-10
Product CodeLLF
DecisionSubstantially Equivalent

Device Summary

ENDOCOAGULATOR MODELS 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 1987-07-10 under 510(k) number K870773. The device is classified under product code LLF. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

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

ENDOCOAGULATOR MODELS 5, 8 & 20 ARGON LASER is a medical device that received FDA 510(k) clearance on 1987-07-10. The listed applicant is Hgm, Inc.. The 510(k) number is K870773.

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

ENDOCOAGULATOR MODELS 5, 8 & 20 ARGON LASER received FDA 510(k) clearance on 1987-07-10, under 510(k) number K870773.

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

The FDA product code for ENDOCOAGULATOR MODELS 5, 8 & 20 ARGON LASER is LLF.

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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: LLF)

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.

K864610CILAS YM 101 ND:YAG LASER FOR NEUROLOGICAL USEInframed, Inc.K860977MODEL 545-45 FOR NEUROLOGICAL SURGICAL APPLICATIONBritt Corp., Inc.K833497COOPER MEDICAL MODEL 770Cooper Medical Corp.

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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