Organ Recovery Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Organ Recovery Systems, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Organ Recovery Systems, Inc. has 4 FDA 510(k) cleared medical devices. Based in Charleston, US.
Historical record: 4 cleared submissions from 2002 to 2010. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Organ Recovery Systems, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Organ Recovery Systems, Inc.
4 devices
Cleared
Mar 11, 2010
SPS-1TM STATIC PRESERVATION SOLUTION, MODELS SPS-1-500 ML, SPS 1-1L, SPS-1-2L
Gastroenterology & Urology
275d
Cleared
Jul 31, 2003
LIFEPORT, KIDNEY PERFUSION TRANSPORTER (KTR)
Gastroenterology & Urology
457d
Cleared
Oct 21, 2002
MODIFICATION TO KPS-1, KIDNEY PERFUSION SOLUTIION
Gastroenterology & Urology
90d
Cleared
Jan 25, 2002
KPS-I, THE KIDNEY PERFUSION SOLUTION
Gastroenterology & Urology
88d