Uresil Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
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.
FDA 510(k) Regulatory Record - Uresil Corp.
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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