Oec-Diasonics, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K9260569600 FLUOROSCOPIC IMAGING SYSTEMJanuary 21, 1993
K924879EP 3000January 4, 1993
K914446UROVIEW 2000, MODIFICATIONJanuary 10, 1992
K896583F.A.S.T. TABLEMarch 1, 1990
K893475UROVIEW IIAugust 10, 1989
K872022UROVIEWJuly 16, 1987
K864837MODIFIED MAINFRAME OF MODEL 902 MOBILE C-ARMJanuary 30, 1987
K843972ANGIOPLUS-SJanuary 3, 1985