Cilco I/a Surgical Pack

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K843319 ↗

FDA Product Code

HQC

Device Class

Class II

Regulation

21 CFR Part 886.4670

Advisory Committee

Ophthalmic

FDA Decision

SESE Substantially Equivalent

• Cystotome, 140-S

  Class I

  FDA 510(k) K840475 Active Cleared 5 Apr 1984

• Cilcor Ophthalmic Instruments

  Class I

  FDA 510(k) K843992 Active Cleared 21 Nov 1984

• Cilco Ascan

  Not classified

  FDA 510(k) K827371 Active Cleared 9 Jul 1982

• Octopus 500/500E

  Class I

  FDA 510(k) K841099 Active Cleared 19 Jun 1984

• Opthalmic Endoscope

  Not classified

  FDA 510(k) K832405 Active Cleared 21 Nov 1983

• Cilco Diamond Knife

  Class I

  FDA 510(k) K843447 Active Cleared 5 Oct 1984

See all devices from Cilco, Inc. →