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FDA 510(k)

ULTRA-WIDE SAFETY SPECTACLE FRAME

K-Number: K813156 · 1981-12-14

ApplicantZee Medical Products Co., Inc.
Decision Date1981-12-14
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ULTRA-WIDE SAFETY SPECTACLE FRAME is the device name listed in this FDA 510(k) record. The listed applicant is Zee Medical Products Co., Inc.. It received FDA 510(k) clearance on 1981-12-14 under 510(k) number K813156. 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 ULTRA-WIDE SAFETY SPECTACLE FRAME?

ULTRA-WIDE SAFETY SPECTACLE FRAME is a medical device that received FDA 510(k) clearance on 1981-12-14. The listed applicant is Zee Medical Products Co., Inc.. The 510(k) number is K813156.

When did ULTRA-WIDE SAFETY SPECTACLE FRAME receive FDA 510(k) clearance?

ULTRA-WIDE SAFETY SPECTACLE FRAME received FDA 510(k) clearance on 1981-12-14, under 510(k) number K813156.

Who is the listed applicant for ULTRA-WIDE SAFETY SPECTACLE FRAME?

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

What is the FDA product code for ULTRA-WIDE SAFETY SPECTACLE FRAME?

The FDA product code for ULTRA-WIDE SAFETY SPECTACLE FRAME is HQZ.

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Other records listing Zee Medical Products 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.

K823501ZEE SPHYGMOMANOMETERK813016ZEE TRACTION SPLINTK812814ZEE SURGICAL INSTRUMENTSK812564ZEE LIFE SUPPORT AIR PANTSK812342ZEE EXTRICATION DEVICEK812284ZEE ELECTRODE-GEL

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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

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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