Cardiotronics, Inc. - FDA 510(k) Cleared Devices
27
Total
27
Cleared
0
Denied
FDA 510(k) Regulatory Record - Cardiotronics, Inc. Cardiovascular ✕
26 devices
Cleared
Feb 24, 1995
EKG VEST
Cardiovascular
618d
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
Cleared
Oct 03, 1991
MODEL #350 SHOCK-PLATE DEFIB ADAPTOR
Cardiovascular
188d