SOLSTAR BRILLENMODE SPECTACLE FRAMES— 510(k) K930561

Name: FDA 510(k) clearance K930561
Creator: U.S. Food and Drug Administration
Published: 1993-05-03

Substantially Equivalent

Solstar Produktions GmbH

FDA 510(k) clearance K930561 for SOLSTAR BRILLENMODE SPECTACLE FRAMES, Substantially Equivalent on 1993-05-03. Applicant: Solstar Produktions GmbH. Device class: 1.

Clearance details

Applicant: Solstar Produktions GmbH
Product code: Code HQZ
Device class: Class 1
Regulation: 21 CFR 886.5842
Advisory panel: Ophthalmic
Date received: 1993-02-03
Decision date: 1993-05-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Austria, AT

Download summary PDF View on FDA.gov ↗

Recent devices under product code HQZ

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K952597 — VIEW POINT, DORION, RUDDY PROJECT, ULTRA FLEX, TRILLON, BAY BOY, SHIELD SKI, SUN POCKETS, POINT OF VIEW1995-09-12
K944313 — SPECTACLE FRAME1995-03-28
K945176 — SPECTACLE FRAME OR EYEGLASS FRAMES1994-12-15
K945392 — SPECTACLE FRAME1994-12-15
K945770 — OPTICAL FRAMES1994-12-15

More clearances from Solstar Produktions GmbH

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K926564 — OPTICAL FRAMES AND SUNGLASSES1994-07-27
K930562 — SOLSTAR BRILLENMODE SUNGLASSES1993-08-17

Data sourced from openFDA. This site is unofficial and independent of the FDA.