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FDA 510(k)

MAX FRAME DESIGN

K-Number: K943913 · 1994-09-07

ApplicantNoble Optic
Decision Date1994-09-07
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MAX FRAME DESIGN is the device name listed in this FDA 510(k) record. The listed applicant is Noble Optic. It received FDA 510(k) clearance on 1994-09-07 under 510(k) number K943913. 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 MAX FRAME DESIGN?

MAX FRAME DESIGN is a medical device that received FDA 510(k) clearance on 1994-09-07. The listed applicant is Noble Optic. The 510(k) number is K943913.

When did MAX FRAME DESIGN receive FDA 510(k) clearance?

MAX FRAME DESIGN received FDA 510(k) clearance on 1994-09-07, under 510(k) number K943913.

Who is the listed applicant for MAX FRAME DESIGN?

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

What is the FDA product code for MAX FRAME DESIGN?

The FDA product code for MAX FRAME DESIGN is HQZ.

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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.

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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