Revivant Corp. - FDA 510(k) Cleared Devices
Recent clearances: AUTOPULSE RESUSCITATION SYSTEM, MODEL 100, MODIFICATION TO: AUTOPULSE RESUSCITATION SYSTEM MODEL 100, AUTOPULSE RESUSCITATION SYSTEM
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Revivant Corp. Cardiovascular ✕
4 devices
Cleared
Mar 11, 2004
AUTOPULSE RESUSCITATION SYSTEM, MODEL 100
Cardiovascular
17d
Cleared
Nov 12, 2003
MODIFICATION TO: AUTOPULSE RESUSCITATION SYSTEM MODEL 100
Cardiovascular
61d
Cleared
Aug 15, 2002
AUTOPULSE RESUSCITATION SYSTEM
Cardiovascular
27d
Cleared
Oct 25, 2001
AUTOPULSE, MODEL 100
Cardiovascular
202d