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FDA 510(k)

HGM ASPIRATING ENDOOCULAR(TM) PROBE

K-Number: K925663 · 1993-08-17

ApplicantHgm, Inc.
Decision Date1993-08-17
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

HGM ASPIRATING ENDOOCULAR(TM) PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Hgm, Inc.. It received FDA 510(k) clearance on 1993-08-17 under 510(k) number K925663. The device is classified under product code HQF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HGM ASPIRATING ENDOOCULAR(TM) PROBE?

HGM ASPIRATING ENDOOCULAR(TM) PROBE is a medical device that received FDA 510(k) clearance on 1993-08-17. The listed applicant is Hgm, Inc.. The 510(k) number is K925663.

When did HGM ASPIRATING ENDOOCULAR(TM) PROBE receive FDA 510(k) clearance?

HGM ASPIRATING ENDOOCULAR(TM) PROBE received FDA 510(k) clearance on 1993-08-17, under 510(k) number K925663.

Who is the listed applicant for HGM ASPIRATING ENDOOCULAR(TM) PROBE?

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 ASPIRATING ENDOOCULAR(TM) PROBE?

The FDA product code for HGM ASPIRATING ENDOOCULAR(TM) PROBE is HQF.

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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 LASERK930543E-25 KRYPTON ION LASER (SURGICA K5)

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Related Devices (Code: HQF)

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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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