Cilco, Inc.
Cilco, Inc. holds FDA 510(k) medical device clearances, first cleared 1982, most recent 1986.
Top product codes for Cilco, Inc.
Recent clearances by Cilco, Inc.
- K861334 — CILCO DIAMOND KNIVES & DIAMOND KNIFE LINEAR GAUGE
- K854969 — CILCO SONOMETRICS A&B DIGITAL SYSTEM (DIGISCAN)
- K844249 — K-SOL
- K843319 — CILCO I/A SURGICAL PACK
- K843992 — CILCOR OPHTHALMIC INSTRUMENTS
- K843447 — CILCO DIAMOND KNIFE
- K841099 — OCTOPUS 500/500E
- K840475 — CYSTOTOME, 140-S
- K832405 — OPTHALMIC ENDOSCOPE
- K827371 — CILCO ASCAN
- K820933 — CILCO I/A HANDPIECE
- K821381 — IOL FORCEPS
Data sourced from openFDA. This site is unofficial and independent of the FDA.