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FDA 510(k)

LAURENT TARDY

K-Number: K903173 · 1990-08-02

ApplicantAcces Intl. Eyewear
Decision Date1990-08-02
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LAURENT TARDY is the device name listed in this FDA 510(k) record. The listed applicant is Acces Intl. Eyewear. It received FDA 510(k) clearance on 1990-08-02 under 510(k) number K903173. 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 LAURENT TARDY?

LAURENT TARDY is a medical device that received FDA 510(k) clearance on 1990-08-02. The listed applicant is Acces Intl. Eyewear. The 510(k) number is K903173.

When did LAURENT TARDY receive FDA 510(k) clearance?

LAURENT TARDY received FDA 510(k) clearance on 1990-08-02, under 510(k) number K903173.

Who is the listed applicant for LAURENT TARDY?

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

What is the FDA product code for LAURENT TARDY?

The FDA product code for LAURENT TARDY 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 Acces Intl. Eyewear 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.

K896350TITAN AIR SPECTACLE FRAME

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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