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510(k) K832405

OPTHALMIC ENDOSCOPE by Cilco, Inc.

K832405 is an FDA 510(k) premarket notification submitted by Cilco, Inc. for the device "OPTHALMIC ENDOSCOPE". The FDA issued a decision of Substantially Equivalent on November 21, 1983. Cilco, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 21, 1983
Date Received
July 21, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Cilco, Inc.

  • K861334 — CILCO DIAMOND KNIVES & DIAMOND KNIFE LINEAR GAUGE (May 2, 1986)
  • K854969 — CILCO SONOMETRICS A&B DIGITAL SYSTEM (DIGISCAN) (February 27, 1986)
  • K844249 — K-SOL (April 30, 1985)
  • K843319 — CILCO I/A SURGICAL PACK (February 14, 1985)
  • K843992 — CILCOR OPHTHALMIC INSTRUMENTS (November 21, 1984)
  • K843447 — CILCO DIAMOND KNIFE (October 5, 1984)
  • K841099 — OCTOPUS 500/500E (June 19, 1984)
  • K840475 — CYSTOTOME, 140-S (April 5, 1984)
  • K827371 — CILCO ASCAN (July 9, 1982)
  • K821381 — IOL FORCEPS (June 14, 1982)

FDA data resources