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FDA 510(k)

EYEGLASS FRAME

K-Number: K940113 · 1994-02-22

ApplicantWan Wing Optical Co.
Decision Date1994-02-22
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

EYEGLASS FRAME is the device name listed in this FDA 510(k) record. The listed applicant is Wan Wing Optical Co.. It received FDA 510(k) clearance on 1994-02-22 under 510(k) number K940113. 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 FRAME?

EYEGLASS FRAME is a medical device that received FDA 510(k) clearance on 1994-02-22. The listed applicant is Wan Wing Optical Co.. The 510(k) number is K940113.

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

EYEGLASS FRAME received FDA 510(k) clearance on 1994-02-22, under 510(k) number K940113.

Who is the listed applicant for EYEGLASS FRAME?

The FDA 510(k) record lists Wan Wing Optical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EYEGLASS FRAME?

The FDA product code for EYEGLASS FRAME 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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