Uresil Corp. - FDA 510(k) Cleared Devices
45
Total
44
Cleared
0
Denied
Uresil Corp. has 44 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 44 cleared submissions from 1981 to 2001.
Browse the FDA 510(k) cleared devices submitted by Uresil Corp. Filter by specialty or product code using the sidebar.
45 devices
Cleared
Jan 04, 2001
GP GENERAL PURPOSE DRAINAGE SET, MINI-PIGTAIL DRAINAGE CATHETER WITH LOCKING...
Gastroenterology & Urology
30d
Cleared
Nov 20, 1998
URESIL VASCU-FLO INFUSION CATHETER
Cardiovascular
298d
Cleared
Sep 10, 1998
URESIL PERCUTANEOUS DRAINAGE CATHETERS WITH HYDROPHILIC COATING
Gastroenterology & Urology
154d
Cleared
Apr 24, 1998
URESIL DILATOR WITH RADIOPAQUE MARKER
Cardiovascular
88d
Cleared
Apr 08, 1998
URESIL NEPHRO-URETERAL STENT
Gastroenterology & Urology
30d
Cleared
Nov 21, 1997
URESIL GUIDEWIRE
Gastroenterology & Urology
134d
Cleared
Aug 29, 1997
URESIL GENERAL PURPOSE DRAINAGE CATHETER, URESIL NEPHROSTOMY CATHETER, URESIL...
Gastroenterology & Urology
50d
Cleared
Sep 08, 1995
URESIL INTRODUCING NEEDLE
Gastroenterology & Urology
21d
Cleared
Jul 10, 1995
URESIL(R) GUIDEWIRE
Cardiovascular
217d
Cleared
Jun 06, 1995
NEPHRO-URETERAL STENT
Gastroenterology & Urology
364d
Cleared
Oct 28, 1994
MINI-OP LAPAROSCOPIC LASSO
General & Plastic Surgery
31d
Cleared
Sep 21, 1994
URESIL DILATOR
Cardiovascular
140d
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