WOODLYN CLASSIC REFRACTOR, PHOROPTOR— 510(k) K874900

Name: FDA 510(k) clearance K874900
Creator: U.S. Food and Drug Administration
Published: 1987-12-23

Substantially Equivalent

Woodlyn, Inc.

FDA 510(k) clearance K874900 for WOODLYN CLASSIC REFRACTOR, PHOROPTOR, Substantially Equivalent on 1987-12-23. Applicant: Woodlyn, Inc.. Device class: 1.

Clearance details

Applicant: Woodlyn, Inc.
Product code: Code HKN
Device class: Class 1
Regulation: 21 CFR 886.1770
Advisory panel: Ophthalmic
Date received: 1987-12-01
Decision date: 1987-12-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Arlington Heights, IL, US

Download summary PDF View on FDA.gov ↗

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