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FDA 510(k)

ARGON FIBER OPTIC CATHETER

K-Number: K827847 · 1983-01-03

ApplicantHgm, Inc.
Decision Date1983-01-03
Product Code
DecisionSubstantially Equivalent

Device Summary

ARGON FIBER OPTIC CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Hgm, Inc.. It received FDA 510(k) clearance on 1983-01-03 under 510(k) number K827847. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARGON FIBER OPTIC CATHETER?

ARGON FIBER OPTIC CATHETER is a medical device that received FDA 510(k) clearance on 1983-01-03. The listed applicant is Hgm, Inc.. The 510(k) number is K827847.

When did ARGON FIBER OPTIC CATHETER receive FDA 510(k) clearance?

ARGON FIBER OPTIC CATHETER received FDA 510(k) clearance on 1983-01-03, under 510(k) number K827847.

Who is the listed applicant for ARGON FIBER OPTIC CATHETER?

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

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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

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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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