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FDA 510(k)

WOODEN SPECTACLE FRAMES

K-Number: K884272 · 1988-12-12

ApplicantWoodwave
Decision Date1988-12-12
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

WOODEN SPECTACLE FRAMES is the device name listed in this FDA 510(k) record. The listed applicant is Woodwave. It received FDA 510(k) clearance on 1988-12-12 under 510(k) number K884272. 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 WOODEN SPECTACLE FRAMES?

WOODEN SPECTACLE FRAMES is a medical device that received FDA 510(k) clearance on 1988-12-12. The listed applicant is Woodwave. The 510(k) number is K884272.

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

WOODEN SPECTACLE FRAMES received FDA 510(k) clearance on 1988-12-12, under 510(k) number K884272.

Who is the listed applicant for WOODEN SPECTACLE FRAMES?

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

What is the FDA product code for WOODEN SPECTACLE FRAMES?

The FDA product code for WOODEN SPECTACLE 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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