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FDA 510(k)

SPECTACLE FRAMES AND SUNGLASSES

K-Number: K934187 · 1994-01-25

ApplicantWah Ming Optical Mfy. , Ltd.
Decision Date1994-01-25
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SPECTACLE FRAMES AND SUNGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Wah Ming Optical Mfy. , Ltd.. It received FDA 510(k) clearance on 1994-01-25 under 510(k) number K934187. 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 SPECTACLE FRAMES AND SUNGLASSES?

SPECTACLE FRAMES AND SUNGLASSES is a medical device that received FDA 510(k) clearance on 1994-01-25. The listed applicant is Wah Ming Optical Mfy. , Ltd.. The 510(k) number is K934187.

When did SPECTACLE FRAMES AND SUNGLASSES receive FDA 510(k) clearance?

SPECTACLE FRAMES AND SUNGLASSES received FDA 510(k) clearance on 1994-01-25, under 510(k) number K934187.

Who is the listed applicant for SPECTACLE FRAMES AND SUNGLASSES?

The FDA 510(k) record lists Wah Ming Optical Mfy. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPECTACLE FRAMES AND SUNGLASSES?

The FDA product code for SPECTACLE FRAMES AND SUNGLASSES 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

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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