WOODLYN CLASSIC LENSMETER— 510(k) K920861

Substantially Equivalent

Woodlyn, Inc.

FDA 510(k) clearance K920861 for WOODLYN CLASSIC LENSMETER, Substantially Equivalent on 1992-07-30. Applicant: Woodlyn, Inc.. Device class: 1.

Clearance details

Applicant: Woodlyn, Inc.
Product code: Code HLM
Device class: Class 1
Regulation: 21 CFR 886.1425
Advisory panel: Ophthalmic
Date received: 1992-02-25
Decision date: 1992-07-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Arlington Heights, IL, US

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More clearances from Woodlyn, Inc.

K931303 — WOODLYN OPERATION MICROSCOPE1993-06-25
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K900477 — WOODLYN CLASSIC SLIT LAMP MODEL SMM1990-02-21
K900478 — WOODLYN FULL APERTURE TRIAL LENS SET1990-02-21
K890992 — WOODLYN OPHTHALMIC PROJECTOR1989-05-17

Data sourced from openFDA. This site is unofficial and independent of the FDA.