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FDA 510(k)

SOLSTAR BRILLENMODE SPECTACLE FRAMES

K-Number: K930561 · 1993-05-03

ApplicantSolstar Produktions GmbH
Decision Date1993-05-03
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SOLSTAR BRILLENMODE SPECTACLE FRAMES is the device name listed in this FDA 510(k) record. The listed applicant is Solstar Produktions GmbH. It received FDA 510(k) clearance on 1993-05-03 under 510(k) number K930561. 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 SOLSTAR BRILLENMODE SPECTACLE FRAMES?

SOLSTAR BRILLENMODE SPECTACLE FRAMES is a medical device that received FDA 510(k) clearance on 1993-05-03. The listed applicant is Solstar Produktions GmbH. The 510(k) number is K930561.

When did SOLSTAR BRILLENMODE SPECTACLE FRAMES receive FDA 510(k) clearance?

SOLSTAR BRILLENMODE SPECTACLE FRAMES received FDA 510(k) clearance on 1993-05-03, under 510(k) number K930561.

Who is the listed applicant for SOLSTAR BRILLENMODE SPECTACLE FRAMES?

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

What is the FDA product code for SOLSTAR BRILLENMODE SPECTACLE FRAMES?

The FDA product code for SOLSTAR BRILLENMODE SPECTACLE FRAMES 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 Solstar Produktions GmbH 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.

K926564OPTICAL FRAMES AND SUNGLASSESK930562SOLSTAR BRILLENMODE 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

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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