VISOPROTECT: OCCULAR SHIELD— 510(k) K850099

Name: FDA 510(k) clearance K850099
Creator: U.S. Food and Drug Administration
Published: 1985-03-20

Substantially Equivalent

Rockway Enterprises, Inc.

FDA 510(k) clearance K850099 for VISOPROTECT: OCCULAR SHIELD, Substantially Equivalent on 1985-03-20. Applicant: Rockway Enterprises, Inc.. Device class: 1.

Clearance details

Applicant: Rockway Enterprises, Inc.
Product code: Code HMP
Device class: Class 1
Regulation: 21 CFR 878.4440
Advisory panel: General, Plastic Surgery
Date received: 1985-01-11
Decision date: 1985-03-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St George, ME, US

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