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FDA 510(k)

BRILLENERZEUGUNG POMBERGER OR MULTIPLE SPEC FRAMES

K-Number: K931911 · 1993-10-01

ApplicantBrillenerzeugung Pomberger
Decision Date1993-10-01
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BRILLENERZEUGUNG POMBERGER OR MULTIPLE SPEC FRAMES is the device name listed in this FDA 510(k) record. The listed applicant is Brillenerzeugung Pomberger. It received FDA 510(k) clearance on 1993-10-01 under 510(k) number K931911. 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 BRILLENERZEUGUNG POMBERGER OR MULTIPLE SPEC FRAMES?

BRILLENERZEUGUNG POMBERGER OR MULTIPLE SPEC FRAMES is a medical device that received FDA 510(k) clearance on 1993-10-01. The listed applicant is Brillenerzeugung Pomberger. The 510(k) number is K931911.

When did BRILLENERZEUGUNG POMBERGER OR MULTIPLE SPEC FRAMES receive FDA 510(k) clearance?

BRILLENERZEUGUNG POMBERGER OR MULTIPLE SPEC FRAMES received FDA 510(k) clearance on 1993-10-01, under 510(k) number K931911.

Who is the listed applicant for BRILLENERZEUGUNG POMBERGER OR MULTIPLE SPEC FRAMES?

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

What is the FDA product code for BRILLENERZEUGUNG POMBERGER OR MULTIPLE SPEC FRAMES?

The FDA product code for BRILLENERZEUGUNG POMBERGER OR MULTIPLE SPEC FRAMES is HQZ.

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Other records listing Brillenerzeugung Pomberger 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.

K931910BRILLENERZEUGUNG POMBERGER OR MULTIPLE SUNGLASSES

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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