Siemens Burdick, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
FDA 510(k) Regulatory Record - Siemens Burdick, Inc. Cardiovascular ✕
5 devices
Cleared
Oct 09, 1992
ELITE II ELECTROCARDIOGRAPH,MODIFIED
Cardiovascular
318d
Cleared
Jul 01, 1992
MEGACART
Cardiovascular
224d
Cleared
May 15, 1992
INTERNAL MODEM FOR THE E560 ELECTROCARDIOGRAPH
Cardiovascular
179d
Cleared
Mar 26, 1992
E350I ELECTROCARDIOGRAPH
Cardiovascular
142d
Cleared
Jul 24, 1991
DC200 DEFIBRILLATOR
Cardiovascular
161d