Woodlyn Classic Cataract Acuity Test

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K843812 ↗

FDA Product Code

HLI

Device Class

Class II

Regulation

21 CFR Part 886.1570

Advisory Committee

Ophthalmic

FDA Decision

SESE Substantially Equivalent

• Woodlyn Standard Slit Lamp Hssl-St

  Class I

  FDA 510(k) K841765 Active Cleared 7 Aug 1984

• Woodlyn Slit Lamp Hssl-Ec

  Class II

  FDA 510(k) K841763 Active Cleared 2 Aug 1984

• Ophthalmic Table

  Class I

  FDA 510(k) K841759 Active Cleared 1 Jun 1984

• Woodlyn Classic Javal Ophthalmometer

  Class II

  FDA 510(k) K841764 Active Cleared 7 Aug 1984

• Woodlyn Classic Lensmeter

  Class I

  FDA 510(k) K920861 Active Cleared 30 Jul 1992

• Woodlyn Slit Lamp Model Hr-1

  Class II

  FDA 510(k) K900476 Active Cleared 21 Feb 1990

See all devices from Woodlyn, Inc. →