Rusch Intl. - FDA 510(k) Cleared Devices
43
Total
43
Cleared
0
Denied
Rusch Intl. has 43 FDA 510(k) cleared medical devices. Based in Jeffrey, US.
Historical record: 43 cleared submissions from 1995 to 2003. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Rusch Intl. Filter by specialty or product code using the sidebar.
43 devices
Cleared
Dec 23, 2003
INTERMITTENT URETHRAL CATHETERS
Gastroenterology & Urology
88d
Cleared
Jun 30, 2003
RUSCH POLYFLEX STENT FOR THE ESOPHAGUS W/INTRODUCER/DELIVERY SYSTEM
Gastroenterology & Urology
129d
Cleared
Jun 17, 2003
RUSCH GUIDED CHOLANGIOGRAPHY CATHETER
Gastroenterology & Urology
229d
Cleared
Mar 28, 2003
RUSCH CRYSTAL CLEAR TRACHEOSTOMY SETS, CUFFED AND CUFFLESS
Anesthesiology
123d
Cleared
Dec 23, 2002
RUSCH MICROLARYNGEAL TUBE
Anesthesiology
24d
Cleared
Aug 01, 2002
RUSCH EDGAR TUBE
Anesthesiology
83d
Cleared
Jul 23, 2002
RUSCH TRACHEOFIX SET, CUFFED AND UNCUFFED
Anesthesiology
55d
Cleared
Jul 01, 2002
RUSCH FLONEIL
Gastroenterology & Urology
118d
Cleared
Feb 26, 2002
RUSCH MILLER-ABBOTT TUBE
Gastroenterology & Urology
347d
Cleared
Feb 26, 2002
RUSCH CANTOR TUBE
Gastroenterology & Urology
347d
Cleared
Feb 12, 2002
RUSCH MEMORY BAG
General & Plastic Surgery
83d
Cleared
Nov 27, 2001
RUSCH POLYFLEX STENT KIT
General & Plastic Surgery
57d
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