PERSOL, MOSCLHINO, AND GERALD GENTA— 510(k) K942845

Name: FDA 510(k) clearance K942845
Creator: U.S. Food and Drug Administration
Published: 1994-08-04

Substantially Equivalent

Persol America, Inc.

FDA 510(k) clearance K942845 for PERSOL, MOSCLHINO, AND GERALD GENTA, Substantially Equivalent on 1994-08-04. Applicant: Persol America, Inc.. Device class: 1.

Clearance details

Applicant: Persol America, Inc.
Product code: Code HQZ
Device class: Class 1
Regulation: 21 CFR 886.5842
Advisory panel: Ophthalmic
Date received: 1994-06-16
Decision date: 1994-08-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Boca Raton, FL, US

Download summary PDF View on FDA.gov ↗

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K945392 — SPECTACLE FRAME1994-12-15
K945770 — OPTICAL FRAMES1994-12-15

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