Revivant Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Revivant Corp. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Revivant Corp. has 4 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.
Historical record: 4 cleared submissions from 2001 to 2004. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Revivant Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Revivant Corp.
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