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FDA 510(k)

VENETO COLLECTION

K-Number: K912034 · 1991-08-22

ApplicantAtlantic Optical Co., Inc.
Decision Date1991-08-22
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

VENETO COLLECTION is the device name listed in this FDA 510(k) record. The listed applicant is Atlantic Optical Co., Inc.. It received FDA 510(k) clearance on 1991-08-22 under 510(k) number K912034. 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 VENETO COLLECTION?

VENETO COLLECTION is a medical device that received FDA 510(k) clearance on 1991-08-22. The listed applicant is Atlantic Optical Co., Inc.. The 510(k) number is K912034.

When did VENETO COLLECTION receive FDA 510(k) clearance?

VENETO COLLECTION received FDA 510(k) clearance on 1991-08-22, under 510(k) number K912034.

Who is the listed applicant for VENETO COLLECTION?

The FDA 510(k) record lists Atlantic Optical Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VENETO COLLECTION?

The FDA product code for VENETO COLLECTION 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 Atlantic Optical Co., 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.

K941555SUNGLASSES/VARIOUS COLLECTIONSK941052EYEGLASS SPECTACLE FRAMES VARIOUS COLLECTIONS

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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