Cathlab Corp. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Cathlab Corp. has 8 FDA 510(k) cleared medical devices. Based in Tustin, US.
Historical record: 8 cleared submissions from 1988 to 1991. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cathlab Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Cathlab Corp.
8 devices
Cleared
Aug 02, 1991
CATHLAB SILICONE BILIARY BALLOON CATHETER
Gastroenterology & Urology
150d
Cleared
Jun 24, 1991
CATHLAB SILICONE OCCLUSION BALLOON CATHETER
Cardiovascular
111d
Cleared
Feb 25, 1991
CATHLAB SILICONE ARTERIAL EMBOLECTOMY CATHETER
Cardiovascular
108d
Cleared
Mar 16, 1990
MILLER PERCUTANEOUS ANGIOGRAPHIC/SCOPIC IRRI. CATH
Cardiovascular
88d
Cleared
Mar 14, 1990
3F AND 4F IRRIGATION EMBOLECTOMY CATHETERS
Cardiovascular
76d
Cleared
Sep 26, 1989
SILICONE FLOW-DIRECTED THERMODILUTION CATHETER
Cardiovascular
147d
Cleared
Aug 01, 1989
SILICONE BI-LUMEN IRRIGATION EMBOLECTOMY CATH.
Cardiovascular
77d
Cleared
Jun 15, 1988
EMBOLECTOMY CATHETER(MODIFIED)
Cardiovascular
70d