Siemens Medical Laboratories, Inc. - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Siemens Medical Laboratories, Inc. has 13 FDA 510(k) cleared radiology devices. Based in Mchenry, US.
Historical record: 13 cleared submissions from 1979 to 1991.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
13 devices
Cleared
May 03, 1991
Z XT RADIATION THERAPY TREATMENT TABLE
Radiology
57d
Cleared
Nov 07, 1990
BEAMVIEW & BEAMVIEW PLUS (AKA PROJECT 743)
Radiology
113d
Cleared
Aug 28, 1989
PATIENT DATA MANAGEMENT SYSTEM (PROJECT 735)
Radiology
70d
Cleared
Sep 19, 1988
MEVATRON, M 2 CLASS
Radiology
75d
Cleared
Feb 18, 1988
SONOLINE CF
Cardiovascular
56d
Cleared
Oct 29, 1986
MEVATRON KD-2
Radiology
131d
Cleared
Feb 21, 1986
MEVAMATIC 3
Radiology
95d
Cleared
Sep 19, 1985
SIEMENS MEVATRON ME
Radiology
72d
Cleared
Aug 18, 1981
MEVATRON 67E
Radiology
29d
Cleared
Nov 16, 1979
MEVATRON 74X MEDICAL LINEAR ACCELERATOR
Radiology
45d
Cleared
May 04, 1979
MEVATRON 74
Radiology
18d
Cleared
Apr 23, 1979
MEVATRON 67
Radiology
13d