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FDA 510(k)

VIEW POINT, DORION, RUDDY PROJECT, ULTRA FLEX, TRILLON, BAY BOY, SHIELD SKI, SUN POCKETS, POINT OF VIEW

K-Number: K952597 · 1995-09-12

ApplicantPoint of View Optical Outlet, Inc.
Decision Date1995-09-12
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

VIEW POINT, DORION, RUDDY PROJECT, ULTRA FLEX, TRILLON, BAY BOY, SHIELD SKI, SUN POCKETS, POINT OF VIEW is the device name listed in this FDA 510(k) record. The listed applicant is Point of View Optical Outlet, Inc.. It received FDA 510(k) clearance on 1995-09-12 under 510(k) number K952597. 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 VIEW POINT, DORION, RUDDY PROJECT, ULTRA FLEX, TRILLON, BAY BOY, SHIELD SKI, SUN POCKETS, POINT OF VIEW?

VIEW POINT, DORION, RUDDY PROJECT, ULTRA FLEX, TRILLON, BAY BOY, SHIELD SKI, SUN POCKETS, POINT OF VIEW is a medical device that received FDA 510(k) clearance on 1995-09-12. The listed applicant is Point of View Optical Outlet, Inc.. The 510(k) number is K952597.

When did VIEW POINT, DORION, RUDDY PROJECT, ULTRA FLEX, TRILLON, BAY BOY, SHIELD SKI, SUN POCKETS, POINT OF VIEW receive FDA 510(k) clearance?

VIEW POINT, DORION, RUDDY PROJECT, ULTRA FLEX, TRILLON, BAY BOY, SHIELD SKI, SUN POCKETS, POINT OF VIEW received FDA 510(k) clearance on 1995-09-12, under 510(k) number K952597.

Who is the listed applicant for VIEW POINT, DORION, RUDDY PROJECT, ULTRA FLEX, TRILLON, BAY BOY, SHIELD SKI, SUN POCKETS, POINT OF VIEW?

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

What is the FDA product code for VIEW POINT, DORION, RUDDY PROJECT, ULTRA FLEX, TRILLON, BAY BOY, SHIELD SKI, SUN POCKETS, POINT OF VIEW?

The FDA product code for VIEW POINT, DORION, RUDDY PROJECT, ULTRA FLEX, TRILLON, BAY BOY, SHIELD SKI, SUN POCKETS, POINT OF VIEW is HQZ.

Related Clinical Trials

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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.

K944313SPECTACLE FRAMESun Hing Optical Manufactory , Ltd.K945770OPTICAL FRAMESRamada Optics, Inc.K945392SPECTACLE FRAMESeo Han Corp., Ltd.K945176SPECTACLE FRAME OR EYEGLASS FRAMESOptipia Trading Co.K945350FRAME, SPECTACLESTaiwan Eva Industrial Co., Inc.K945342MAG-1 SPECTACLE FRAMECriss Optical Mfg. 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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