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FDA 510(k)

SEIKO EYEGLASS FRAME

K-Number: K942513 · 1994-07-15

ApplicantSeiko Optical Products of America, Inc.
Decision Date1994-07-15
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SEIKO EYEGLASS FRAME is the device name listed in this FDA 510(k) record. The listed applicant is Seiko Optical Products of America, Inc.. It received FDA 510(k) clearance on 1994-07-15 under 510(k) number K942513. 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 SEIKO EYEGLASS FRAME?

SEIKO EYEGLASS FRAME is a medical device that received FDA 510(k) clearance on 1994-07-15. The listed applicant is Seiko Optical Products of America, Inc.. The 510(k) number is K942513.

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

SEIKO EYEGLASS FRAME received FDA 510(k) clearance on 1994-07-15, under 510(k) number K942513.

Who is the listed applicant for SEIKO EYEGLASS FRAME?

The FDA 510(k) record lists Seiko Optical Products of America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SEIKO EYEGLASS FRAME?

The FDA product code for SEIKO EYEGLASS FRAME is HQZ.

Related Clinical Trials

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.

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Other records listing Seiko Optical Products of America, Inc. as applicant

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.

K900764SUNGLASS, NON-PRESCRIPTIONK873245AR DIACOAT SINGLE VISION LENSESK861684SEIKO P-2 & SEIKO P-3 (SPECTACLE LENS)

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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