WOODLYN LIGHTWEIGHT TRIAL FRAME— 510(k) K841768

Substantially Equivalent

Woodlyn, Inc.

FDA 510(k) clearance K841768 for WOODLYN LIGHTWEIGHT TRIAL FRAME, Substantially Equivalent on 1984-06-01. Applicant: Woodlyn, Inc.. Device class: 1.

Clearance details

Applicant
Woodlyn, Inc.
Product code
Code HPA
Device class
Class 1
Regulation
21 CFR 886.1415
Advisory panel
Ophthalmic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Mchenry, IL, US
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