Cilco, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
12
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K861334CILCO DIAMOND KNIVES & DIAMOND KNIFE LINEAR GAUGEMay 2, 1986
K854969CILCO SONOMETRICS A&B DIGITAL SYSTEM (DIGISCAN)February 27, 1986
K844249K-SOLApril 30, 1985
K843319CILCO I/A SURGICAL PACKFebruary 14, 1985
K843992CILCOR OPHTHALMIC INSTRUMENTSNovember 21, 1984
K843447CILCO DIAMOND KNIFEOctober 5, 1984
K841099OCTOPUS 500/500EJune 19, 1984
K840475CYSTOTOME, 140-SApril 5, 1984
K832405OPTHALMIC ENDOSCOPENovember 21, 1983
K827371CILCO ASCANJuly 9, 1982
K821381IOL FORCEPSJune 14, 1982
K820933CILCO I/A HANDPIECEJune 14, 1982