WOODLYN OPHTHALMIC PROJECTOR— 510(k) K890992

Substantially Equivalent

Woodlyn, Inc.

FDA 510(k) clearance K890992 for WOODLYN OPHTHALMIC PROJECTOR, Substantially Equivalent on 1989-05-17. Applicant: Woodlyn, Inc.. Device class: 1.

Clearance details

Applicant: Woodlyn, Inc.
Product code: Code HOS
Device class: Class 1
Regulation: 21 CFR 886.1680
Advisory panel: Ophthalmic
Date received: 1989-02-27
Decision date: 1989-05-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Arlington Heights, IL, US

Download summary PDF View on FDA.gov ↗

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K862519 — BAUSCH & LOMB ACCU-CHART 3 ACUITY PROJECTOR1986-07-23

More clearances from Woodlyn, Inc.

K931303 — WOODLYN OPERATION MICROSCOPE1993-06-25
K920861 — WOODLYN CLASSIC LENSMETER1992-07-30
K900476 — WOODLYN SLIT LAMP MODEL HR-11990-02-21
K900477 — WOODLYN CLASSIC SLIT LAMP MODEL SMM1990-02-21
K900478 — WOODLYN FULL APERTURE TRIAL LENS SET1990-02-21

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