Electro-Catheter Corp. - FDA 510(k) Cleared Devices
35
Total
35
Cleared
0
Denied
Electro-Catheter Corp. has 35 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.
Historical record: 35 cleared submissions from 1976 to 1995.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Electro-Catheter Corp.
35 devices
Cleared
Jul 27, 1995
MULTIPACE
Cardiovascular
660d
Cleared
Apr 19, 1995
CLOSED TIP MULTI-ELECTRODE CATHETER, MODIFICATION
Cardiovascular
646d
Cleared
Apr 19, 1995
OPEN TIP MULTI-ELECTRODE CATHETER, MODIFICATION
Cardiovascular
646d
Cleared
Apr 19, 1995
TIP DEFLECTOR (GENESIS)
Cardiovascular
287d
Cleared
Feb 24, 1995
SILICORE SEMI-FLOATER
Cardiovascular
507d
Cleared
Apr 29, 1988
ELECATH(R) TRANSESOPHAGEAL PACING CATHETER
Gastroenterology & Urology
199d
Cleared
Feb 10, 1986
ELECATH PERCUTANEOUS LEFT ATRIAL CANNULATION SET
Cardiovascular
90d
Cleared
Jan 15, 1986
ELECATH PULSATILE PERFUSION PUMP
Cardiovascular
34d
Cleared
Apr 10, 1985
ELECATH TORKFLOAT PACING PROBE
Cardiovascular
92d
Cleared
Mar 27, 1985
ELECATH OPEN TIP BIPOLAR PACING CATHETER
Cardiovascular
58d
Cleared
Mar 06, 1985
ELECATH CARDIAC OUTPUT COMPUTER
Cardiovascular
96d
Cleared
Jan 02, 1985
ELECATH GALLAGHER MAPPING CATHETER
Cardiovascular
22d