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FDA 510(k)

SPECTACLE FRAMES+ SUNGLASSSES(NON PRESC.)

K-Number: K914954 · 1992-02-27

ApplicantJsu Corp.
Decision Date1992-02-27
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SPECTACLE FRAMES+ SUNGLASSSES(NON PRESC.) is the device name listed in this FDA 510(k) record. The listed applicant is Jsu Corp.. It received FDA 510(k) clearance on 1992-02-27 under 510(k) number K914954. 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+ SUNGLASSSES(NON PRESC.)?

SPECTACLE FRAMES+ SUNGLASSSES(NON PRESC.) is a medical device that received FDA 510(k) clearance on 1992-02-27. The listed applicant is Jsu Corp.. The 510(k) number is K914954.

When did SPECTACLE FRAMES+ SUNGLASSSES(NON PRESC.) receive FDA 510(k) clearance?

SPECTACLE FRAMES+ SUNGLASSSES(NON PRESC.) received FDA 510(k) clearance on 1992-02-27, under 510(k) number K914954.

Who is the listed applicant for SPECTACLE FRAMES+ SUNGLASSSES(NON PRESC.)?

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

What is the FDA product code for SPECTACLE FRAMES+ SUNGLASSSES(NON PRESC.)?

The FDA product code for SPECTACLE FRAMES+ SUNGLASSSES(NON PRESC.) 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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