Four Modifications to Ophthalas Argon/Dye Laser

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K881494 ↗

FDA Product Code

HQF

Device Class

Class II

Regulation

21 CFR Part 886.4390

Advisory Committee

Ophthalmic

FDA Decision

SN

• Needle or Cutter

  Class II

  FDA 510(k) K953399 Active Cleared 30 Oct 1995

• Paxial

  Class II

  FDA 510(k) K853116 Active Cleared 31 Oct 1985

• Indirect Ophthalmoscope Accessory Delivery System

  Class II

  FDA 510(k) K890509 Active Cleared 24 Mar 1989

• Sterile Disposable Endocular Probe

  Class II

  FDA 510(k) K884456 Active Cleared 9 Dec 1988

• Ophthalas Dye Ophthalmic Laser

  Class II

  FDA 510(k) K873460 Active Cleared 29 Oct 1987

• Interconn. of Ophthalas & Nanolas Laser System

  Class II

  FDA 510(k) K883719 Active Cleared 18 Oct 1988

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