Interventional Therapeutics Corp. - FDA 510(k) Cleared Devices
28
Total
27
Cleared
0
Denied
Interventional Therapeutics Corp. has 27 FDA 510(k) cleared medical devices. Based in Santa Barbara, US.
Historical record: 27 cleared submissions from 1987 to 1996. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Interventional Therapeutics Corp. Filter by specialty or product code using the sidebar.
28 devices
Cleared
May 29, 1996
OCCLUSION BALLOON CATHETER
Cardiovascular
90d
Cleared
Oct 05, 1995
CATHETER, BALLOON TYPE
Cardiovascular
246d
Cleared
Feb 10, 1995
DISPOSABLE 1CC SYRINGE WITH LUER LOCK
General Hospital
88d
Cleared
Dec 13, 1994
CONTOUR EMBOLI
Neurology
105d
Cleared
Nov 17, 1993
INTHERM SINGLE-STICK RADIALLY EXPANDING DILATOR
Gastroenterology & Urology
294d
Cleared
Nov 09, 1993
ITC CONTOUR EMBOLI, MODIFICATION
Neurology
742d
Cleared
Sep 28, 1993
INTHERM STASIS VALVE SYSTEM
Gastroenterology & Urology
211d
Cleared
Jul 23, 1993
INTHERM SINGLE-STICK RADIALLY EXPANDING DILATOR
General & Plastic Surgery
137d
Cleared
Apr 30, 1993
ITC CATHETERS W/ HYDROMER
Cardiovascular
332d
Cleared
Apr 15, 1993
ITC BUNJI PLATINUM EMBOLIZATION COIL
Neurology
147d
Cleared
Mar 23, 1993
ITC BUNJI PLATINUM EMBOLIZATION COIL
Neurology
141d
Cleared
Feb 12, 1993
ANGIOGRAPHIC CATHETER -- MODIFICATION
Cardiovascular
282d