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FDA 510(k)

OPTHLAMIC FRAMES

K-Number: K910951 · 1991-05-06

ApplicantUnited Optical, Spa
Decision Date1991-05-06
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OPTHLAMIC FRAMES is the device name listed in this FDA 510(k) record. The listed applicant is United Optical, Spa. It received FDA 510(k) clearance on 1991-05-06 under 510(k) number K910951. The device is classified under product code HQZ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPTHLAMIC FRAMES?

OPTHLAMIC FRAMES is a medical device that received FDA 510(k) clearance on 1991-05-06. The listed applicant is United Optical, Spa. The 510(k) number is K910951.

When did OPTHLAMIC FRAMES receive FDA 510(k) clearance?

OPTHLAMIC FRAMES received FDA 510(k) clearance on 1991-05-06, under 510(k) number K910951.

Who is the listed applicant for OPTHLAMIC FRAMES?

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

What is the FDA product code for OPTHLAMIC FRAMES?

The FDA product code for OPTHLAMIC FRAMES is HQZ.

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Related Devices (Code: HQZ)

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.

K952597VIEW POINT, DORION, RUDDY PROJECT, ULTRA FLEX, TRILLON, BAY BOY, SHIELD SKI, SUN POCKETS, POINT OF VIEWPoint of View Optical Outlet, Inc.K944313SPECTACLE FRAMESun Hing Optical Manufactory , Ltd.K945392SPECTACLE FRAMESeo Han Corp., Ltd.K945176SPECTACLE FRAME OR EYEGLASS FRAMESOptipia Trading Co.K945770OPTICAL FRAMESRamada Optics, Inc.K945350FRAME, SPECTACLESTaiwan Eva Industrial Co., Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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