SUNGLASSES— 510(k) K945920

Name: FDA 510(k) clearance K945920
Creator: U.S. Food and Drug Administration
Published: 1995-01-17

Substantially Equivalent

Glendale Protective Technologies, Inc.

FDA 510(k) clearance K945920 for SUNGLASSES, Substantially Equivalent on 1995-01-17. Applicant: Glendale Protective Technologies, Inc.. Device class: 1.

Clearance details

Applicant: Glendale Protective Technologies, Inc.
Product code: Code HQY
Device class: Class 1
Regulation: 21 CFR 886.5850
Advisory panel: Ophthalmic
Date received: 1994-12-05
Decision date: 1995-01-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lakeland, FL, US

Download summary PDF View on FDA.gov ↗

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