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FDA 510(k)

PAUL SMITH SPECTACLES LTD. BY OLIVER PEOPLES, INC.

K-Number: K942348 · 1994-07-12

ApplicantOliver Peoples, Inc.
Decision Date1994-07-12
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PAUL SMITH SPECTACLES LTD. BY OLIVER PEOPLES, INC. is the device name listed in this FDA 510(k) record. The listed applicant is Oliver Peoples, Inc.. It received FDA 510(k) clearance on 1994-07-12 under 510(k) number K942348. 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 PAUL SMITH SPECTACLES LTD. BY OLIVER PEOPLES, INC.?

PAUL SMITH SPECTACLES LTD. BY OLIVER PEOPLES, INC. is a medical device that received FDA 510(k) clearance on 1994-07-12. The listed applicant is Oliver Peoples, Inc.. The 510(k) number is K942348.

When did PAUL SMITH SPECTACLES LTD. BY OLIVER PEOPLES, INC. receive FDA 510(k) clearance?

PAUL SMITH SPECTACLES LTD. BY OLIVER PEOPLES, INC. received FDA 510(k) clearance on 1994-07-12, under 510(k) number K942348.

Who is the listed applicant for PAUL SMITH SPECTACLES LTD. BY OLIVER PEOPLES, INC.?

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

What is the FDA product code for PAUL SMITH SPECTACLES LTD. BY OLIVER PEOPLES, INC.?

The FDA product code for PAUL SMITH SPECTACLES LTD. BY OLIVER PEOPLES, INC. 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 Oliver Peoples, 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.

K923500BEAUSOLEIL 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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