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FDA 510(k)

SPECTACLE FRAMES, READING GLASSES

K-Number: K941463 · 1994-06-17

ApplicantWell Arts Optical Factory , Ltd.
Decision Date1994-06-17
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SPECTACLE FRAMES, READING GLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Well Arts Optical Factory , Ltd.. It received FDA 510(k) clearance on 1994-06-17 under 510(k) number K941463. 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, READING GLASSES?

SPECTACLE FRAMES, READING GLASSES is a medical device that received FDA 510(k) clearance on 1994-06-17. The listed applicant is Well Arts Optical Factory , Ltd.. The 510(k) number is K941463.

When did SPECTACLE FRAMES, READING GLASSES receive FDA 510(k) clearance?

SPECTACLE FRAMES, READING GLASSES received FDA 510(k) clearance on 1994-06-17, under 510(k) number K941463.

Who is the listed applicant for SPECTACLE FRAMES, READING GLASSES?

The FDA 510(k) record lists Well Arts Optical Factory , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPECTACLE FRAMES, READING GLASSES?

The FDA product code for SPECTACLE FRAMES, READING GLASSES 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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