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Siemens Medical Corp.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K012202NUMARIS 4VA15ASeptember 27, 2001
K010721AXIOM ARTIS MODULAR ANGIOGRAPHY SYSTEMMarch 30, 2001
K994231SIEMENS INTEGRATED OPERATING SYSTEM (SIOS)August 10, 2000
K994316MAGNETOM OPEN VIVA WITH PERMANENT MAGNETJanuary 14, 2000
K9846343D-ANGIOMarch 12, 1999