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Kera Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K901009MODEL 2000 INTRAOPERATIVE CORNEASCOPEMay 30, 1990
K871479VIDEOSCAN (TM)May 22, 1987
K864037KERASCAN MODEL 2000 KERATOGRAPHIC AUTO ANALYZERNovember 13, 1986
K850665CORNEASCOPE MODEL 1200March 20, 1985