Cooper Medical Devices Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K802971LANDERS CONTACT LENSFebruary 5, 1981
K802927SEBESTYEN IRRIGATING CONTACT LENSFebruary 5, 1981
K801850CHARLES PNEUMATIC INTRAOCULAR SCISSORSSeptember 16, 1980
K801411MAY ILLUMINATED/INFUSION PICJuly 21, 1980
K801312THE PROTECTORSJune 17, 1980
K800833VABRA ASPIRATORMay 14, 1980
K791898OCUTOME MODEL 8000October 30, 1979