WINK-EASE PERSONAL PROTECTIVE EYEWEAR— 510(k) K873662

Name: FDA 510(k) clearance K873662
Creator: U.S. Food and Drug Administration
Published: 1987-10-02

Substantially Equivalent

Eye Pro Medical Products, Inc.

FDA 510(k) clearance K873662 for WINK-EASE PERSONAL PROTECTIVE EYEWEAR, Substantially Equivalent on 1987-10-02. Applicant: Eye Pro Medical Products, Inc.. Device class: 1.

Clearance details

Applicant: Eye Pro Medical Products, Inc.
Product code: Code HOY
Device class: Class 1
Regulation: 21 CFR 886.4750
Advisory panel: Ophthalmic
Date received: 1987-09-10
Decision date: 1987-10-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Indianapolis, IN, US

Download summary PDF View on FDA.gov ↗

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