Cardiotronics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardiotronics, Inc. - FDA 510(k) Cleared Devices
27
Total
27
Cleared
0
Denied
Cardiotronics, Inc. has 27 FDA 510(k) cleared cardiovascular devices. Based in West Carlsbad, US.
Historical record: 27 cleared submissions from 1988 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 - Cardiotronics, Inc.
27 devices
Cleared
Feb 24, 1995
EKG VEST
Cardiovascular
618d
Cleared
Dec 01, 1992
MODEL #510 STEALTH-PLATE DISPERSIVE ELECTRODE
Neurology
211d
Cleared
Sep 18, 1992
MODEL #340 STEALTH-TRODE+LS
Cardiovascular
74d
Cleared
Jun 11, 1992
MODEL # 230 ST STEALTH-TRODE DEFIB PADS (STERILE)
Cardiovascular
34d
Cleared
Jun 11, 1992
MODEL # 830 ST ADULT STIMULATION PADS (STERILE)
Cardiovascular
34d
Cleared
Jun 11, 1992
MODEL #225-ST SHOCK-TRODE ADULT DEFIB PADS STERILE
Cardiovascular
30d
Cleared
May 26, 1992
MODEL #125 CHILD STIMULATION PADS
Cardiovascular
53d
Cleared
Feb 03, 1992
SHOCK-PATCH ADULT DEFIBRILLATION PADS
Cardiovascular
26d
Cleared
Nov 05, 1991
COORDINATOR, CABLE INPUT
Cardiovascular
15d
Cleared
Oct 16, 1991
MODEL #100 SHOCK-TRODE CHILD DEFIB PADS
Cardiovascular
196d
Cleared
Oct 16, 1991
MODEL #110 STEALTH-TRODE CHILD DEFIB PADS
Cardiovascular
196d
Cleared
Oct 16, 1991
MODEL #911 STEALTH MULTI PADS
Cardiovascular
125d