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FDA 510(k)

GAMP & ASSOC. DISPOSABLE ENDOOCULAR LASER PROBE

K-Number: K954307 · 1995-12-22

ApplicantGamp & Assoc.
Decision Date1995-12-22
Product CodeHQB
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

GAMP & ASSOC. DISPOSABLE ENDOOCULAR LASER PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Gamp & Assoc.. It received FDA 510(k) clearance on 1995-12-22 under 510(k) number K954307. The device is classified under product code HQB. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GAMP & ASSOC. DISPOSABLE ENDOOCULAR LASER PROBE?

GAMP & ASSOC. DISPOSABLE ENDOOCULAR LASER PROBE is a medical device that received FDA 510(k) clearance on 1995-12-22. The listed applicant is Gamp & Assoc.. The 510(k) number is K954307.

When did GAMP & ASSOC. DISPOSABLE ENDOOCULAR LASER PROBE receive FDA 510(k) clearance?

GAMP & ASSOC. DISPOSABLE ENDOOCULAR LASER PROBE received FDA 510(k) clearance on 1995-12-22, under 510(k) number K954307.

Who is the listed applicant for GAMP & ASSOC. DISPOSABLE ENDOOCULAR LASER PROBE?

The FDA 510(k) record lists Gamp & Assoc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GAMP & ASSOC. DISPOSABLE ENDOOCULAR LASER PROBE?

The FDA product code for GAMP & ASSOC. DISPOSABLE ENDOOCULAR LASER PROBE is HQB.

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Other records listing Gamp & Assoc. 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.

K952569GAMP & ASSOCIATES THREE FUNCTION DISPOSABLE MANIPULATORK952581GAMP & ASSOCIATES DISPOSABLE FIBEROPTIC VISCOINJECTORK952585GAMP & ASSOCIATES DISPOSABLE END IRRIGATING ENDOILLUMINATORK954308GAMP & ASSOC. DISPOSABLE ASPIRATING ENDOOCULAR LASER PROBEK954306GAMP & ASSOC. DISPOSABLE ILL ENDOCULAR LASER PROBEK952584GAMP & ASSOCIATES DISPOSABLE ENDOILLUMINATOR W/PICK

View all 9 devices →

Related Devices (Code: HQB)

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.

K220263Vortex Surgical Laser Probes, Vortex Surgical Illuminated Laser Probes, Vortex Surgical Endoilluminators, Vortex Surgical ChandeliersVortex Surgical, Inc.K191846MAXReach Laser ProbeVortex Surgical, Inc.K182646Vitreq disposable laser probes, light fibers and ChandelierVitreQ BVK132614PEREGRINE CURVED ILLUMINATING LASER PROBEPeregrine Surgical , Ltd.K12299723GA CURVED ILLUMINATING LASER PROBEPeregrine Surgical , Ltd.K122905PEREGRINE 23GA CURVED LASER PROBEPeregrine Surgical , Ltd.

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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