SOLSTAR BRILLENMODE SUNGLASSES— 510(k) K930562

Name: FDA 510(k) clearance K930562
Creator: U.S. Food and Drug Administration
Published: 1993-08-17

Substantially Equivalent

Solstar Produktions GmbH

FDA 510(k) clearance K930562 for SOLSTAR BRILLENMODE SUNGLASSES, Substantially Equivalent on 1993-08-17. Applicant: Solstar Produktions GmbH. Device class: 1.

Clearance details

Applicant: Solstar Produktions GmbH
Product code: Code HQY
Device class: Class 1
Regulation: 21 CFR 886.5850
Advisory panel: Ophthalmic
Date received: 1993-02-03
Decision date: 1993-08-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Austria, AT

Download summary PDF View on FDA.gov ↗

Recent devices under product code HQY

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K974852 — NON-PRESCRIPTION SUNGLASSES1998-01-30
K974860 — NON-PRESCRIPTION SUNGLASSES1998-01-30
K974861 — NON-PRESCRIPTION SUNGLASSES1998-01-27
K974511 — SUNGLASSES1998-01-12
K974441 — SUNGLASSES1998-01-09

More clearances from Solstar Produktions GmbH

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K926564 — OPTICAL FRAMES AND SUNGLASSES1994-07-27
K930561 — SOLSTAR BRILLENMODE SPECTACLE FRAMES1993-05-03

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