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FDA 510(k)

SOLEX & SAXON INT'L OPTICAL OF HONG KONG

K-Number: K851661 · 1985-05-30

ApplicantSouth West Intl., Inc.
Decision Date1985-05-30
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SOLEX & SAXON INT'L OPTICAL OF HONG KONG is the device name listed in this FDA 510(k) record. The listed applicant is South West Intl., Inc.. It received FDA 510(k) clearance on 1985-05-30 under 510(k) number K851661. 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 SOLEX & SAXON INT'L OPTICAL OF HONG KONG?

SOLEX & SAXON INT'L OPTICAL OF HONG KONG is a medical device that received FDA 510(k) clearance on 1985-05-30. The listed applicant is South West Intl., Inc.. The 510(k) number is K851661.

When did SOLEX & SAXON INT'L OPTICAL OF HONG KONG receive FDA 510(k) clearance?

SOLEX & SAXON INT'L OPTICAL OF HONG KONG received FDA 510(k) clearance on 1985-05-30, under 510(k) number K851661.

Who is the listed applicant for SOLEX & SAXON INT'L OPTICAL OF HONG KONG?

The FDA 510(k) record lists South West Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SOLEX & SAXON INT'L OPTICAL OF HONG KONG?

The FDA product code for SOLEX & SAXON INT'L OPTICAL OF HONG KONG 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 South West Intl., 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.

K862503KOELN OPTIKK862502MASUNAGA OPTICAL MANUFACTURINGK854343SIOM

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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