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FDA 510(k)

EYEGLASS FRAMES

K-Number: K810278 · 1981-04-03

ApplicantCaesar Intl. Designs
Decision Date1981-04-03
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

EYEGLASS FRAMES is the device name listed in this FDA 510(k) record. The listed applicant is Caesar Intl. Designs. It received FDA 510(k) clearance on 1981-04-03 under 510(k) number K810278. 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 EYEGLASS FRAMES?

EYEGLASS FRAMES is a medical device that received FDA 510(k) clearance on 1981-04-03. The listed applicant is Caesar Intl. Designs. The 510(k) number is K810278.

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

EYEGLASS FRAMES received FDA 510(k) clearance on 1981-04-03, under 510(k) number K810278.

Who is the listed applicant for EYEGLASS FRAMES?

The FDA 510(k) record lists Caesar Intl. Designs as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EYEGLASS FRAMES?

The FDA product code for EYEGLASS 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.K945770OPTICAL FRAMESRamada Optics, Inc.K945392SPECTACLE FRAMESeo Han Corp., Ltd.K945176SPECTACLE FRAME OR EYEGLASS FRAMESOptipia Trading Co.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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