Oec-Diasonics, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Oec-Diasonics, Inc. has 8 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Historical record: 8 cleared submissions from 1985 to 1993. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Oec-Diasonics, Inc. Filter by specialty or product code using the sidebar.
8 devices
Cleared
Jan 21, 1993
9600 FLUOROSCOPIC IMAGING SYSTEM
Radiology
51d
Cleared
Jan 04, 1993
EP 3000
Radiology
98d
Cleared
Jan 10, 1992
UROVIEW 2000, MODIFICATION
Radiology
98d
Cleared
Mar 01, 1990
F.A.S.T. TABLE
Radiology
100d
Cleared
Aug 10, 1989
UROVIEW II
Radiology
98d
Cleared
Jul 16, 1987
UROVIEW
Gastroenterology & Urology
51d
Cleared
Jan 30, 1987
MODIFIED MAINFRAME OF MODEL 902 MOBILE C-ARM
Radiology
52d
Cleared
Jan 03, 1985
ANGIOPLUS-S
Radiology
84d