Katecho, Inc. - FDA 510(k) Cleared Devices
26
Total
25
Cleared
0
Denied
FDA 510(k) Regulatory Record - Katecho, Inc. Cardiovascular ✕
17 devices
Cleared
Oct 12, 2001
K-DEFIB/PACE ADULT ELECTRODE, MODEL KDP-85
Cardiovascular
74d
Cleared
Dec 14, 2000
K-DEFIB/PACE MULTIFUCTION PEDIATRIC ELECTRODE, MODEL KDP-70A
Cardiovascular
59d
Cleared
Nov 21, 2000
K-DEFIB/PACE, MODEL KDP-60A
Cardiovascular
74d
Cleared
Feb 03, 2000
K-DEFIB/PACE ADULT ELECTRODE, MODEL KDP-80
Cardiovascular
90d
Cleared
Aug 23, 1999
K-DEFIB/PACE RADIOLUCENT ADULT ELECTRODE, MODEL KRT-60
Cardiovascular
150d
Cleared
Dec 09, 1998
K-DEFIB/PACE ADULT ELECTRODE MODEL NUMBER KDP-60
Cardiovascular
205d
Cleared
Nov 17, 1995
K-DEFIB/PACE PEDIATRIC ELECTRODE
Cardiovascular
50d
Cleared
Jan 24, 1995
K-DEFIB/PACE PEDIATRIC ELECTRODE
Cardiovascular
481d
Cleared
Aug 03, 1994
K-KLIP
Cardiovascular
162d
Cleared
Jul 25, 1994
PEDIATRIC DEFIB K-PADS
Cardiovascular
273d
Cleared
Jun 09, 1994
K-SNAP
Cardiovascular
121d
Cleared
Apr 15, 1993
K-DEFIB/PACE CARBON ELECTRODE
Cardiovascular
128d
Cleared
Jun 29, 1992
GEL-TAC
Cardiovascular
216d
Cleared
May 14, 1992
K-DEFIB/PACE ELECTRODE
Cardiovascular
191d
Cleared
Jul 30, 1991
K-FREE
Cardiovascular
48d
Cleared
Jan 18, 1990
DEFIB K-PADS
Cardiovascular
120d
Cleared
Nov 12, 1986
K-STIK DEFIBRILLATION PADS
Cardiovascular
36d