Coburn Optical Ind., Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
14
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K892351MAGNILINK SYSTEM 602May 26, 1989
K892348MAGNILINK SYSTEM 201May 26, 1989
K892350MAGNILINK SYSTEM 402/5May 26, 1989
K892349MAGNILINK SYSTEM 209May 26, 1989
K892347MAGNILINK SYSTEM 101May 26, 1989
K862188IRRIGATION & ASPIRATION/VITRECTOMY DEVICEAugust 21, 1986
K853457COBURN I/A SYSTEMOctober 15, 1985
K821737DISP. MICROSURGICAL KNIVESJuly 2, 1982
K812441DI-CROWNOctober 6, 1981
K803159AUTOMATED PERIMETERSFebruary 4, 1981
K801659BIOPHTAL CLINICAL ENDOTHELIAL MICROSCOPESeptember 9, 1980
K801231EYE-VACJuly 21, 1980
K791659MEDITEC (RODENSTOCK) LASER PHOTOCOAGULOctober 11, 1979
K781507RETINOMETERNovember 15, 1978