Rusch, Inc. - FDA 510(k) Cleared Devices
26
Total
24
Cleared
0
Denied
Rusch, Inc. has 24 FDA 510(k) cleared medical devices. Based in Jeffrey, US.
Historical record: 24 cleared submissions from 1993 to 2001. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Rusch, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Rusch, Inc.
26 devices
Cleared
May 09, 2001
RUSCH MMG/O'NEIL CATHETER
Gastroenterology & Urology
86d
Cleared
May 31, 2000
RUSCH EMERGENCY MASK
Anesthesiology
226d
Cleared
Mar 24, 2000
RUSCH MANUAL RESUSCITATOR BAG
Anesthesiology
183d
Cleared
Jun 09, 1998
RUSCH SILICONE FOLEY CATHETER
Gastroenterology & Urology
97d
Cleared
Jan 27, 1998
RUSCH SIMPLASTIC COUNCILL TIP CATHETER
Gastroenterology & Urology
64d
Cleared
May 23, 1997
RUSCH ENTERAL FEEDING TUBE
Gastroenterology & Urology
245d
Cleared
Feb 07, 1997
RUSCH SUPRAPUBIC TRAY
Gastroenterology & Urology
35d
Cleared
Dec 17, 1996
RUSCH SIMPLASTIC FOLEY CATHETERIZATION SET
Gastroenterology & Urology
74d
Cleared
Jun 28, 1996
RUSCH ULTRA TRACHEOFLEX TRACHEOSTOMY SET, CUFFED, STERILE
Anesthesiology
205d
Cleared
Jun 27, 1996
RUSCH REINFORCED TRACHAEL TUBE CUFFED, STERILE
Anesthesiology
209d
Cleared
Nov 27, 1995
RUSCH SINGLE LUMEN BRONCHIAL TUVBE SET, STERILE, FOR LEFT & RIGHT SIDED...
Anesthesiology
97d
Cleared
Nov 21, 1995
LOW PROFILE CATHETER
Gastroenterology & Urology
1268d