Keeler Optical Products , Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K810403KEELER/KONAN SPECULAR MICROSCOPEMay 13, 1981
K801418KEELER AMOILS ACULL CRYO OPHTHALMIC UNITJuly 21, 1980
K792255NEVYAS AUTOPRESS EYE COMPRESSORDecember 11, 1979
K782141LEVIGATOR, KEELER PHOKOJanuary 26, 1979
K781892LOCATOR, FOREIGN BODYDecember 4, 1978