Medical Device Manufacturer · US , Des Moines , IA

Katecho, Inc. - FDA 510(k) Cleared Devices

26 submissions · 25 cleared · Since 1984
26
Total
25
Cleared
0
Denied

Katecho, Inc. has 25 FDA 510(k) cleared medical devices. Based in Des Moines, US.

Historical record: 25 cleared submissions from 1984 to 2001. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Katecho, Inc. Filter by specialty or product code using the sidebar.

26 devices
1–12 of 26
K-DEFIB/PACE ADULT ELECTRODE, MODEL KDP-85
K012404 · DRO Pacemaker, Cardiac, External Transcutaneous (non-invasive) · Cardiovascular
Oct 2001 74d
KM-30 TENS ELECTRODE
K010543 · GXY Electrode, Cutaneous · Neurology
May 2001 89d
K-DEFIB/PACE MULTIFUCTION PEDIATRIC ELECTRODE, MODEL KDP-70A
K003228 · MKJ Automated External Defibrillators (non-wearable) · Cardiovascular
Dec 2000 59d
K-DEFIB/PACE, MODEL KDP-60A
K002806 · MKJ Automated External Defibrillators (non-wearable) · Cardiovascular
Nov 2000 74d
KM-10 TENS ELECTRODE
K000870 · GXY Electrode, Cutaneous · Neurology
Nov 2000 232d
K-DEFIB/PACE ADULT ELECTRODE, MODEL KDP-80
K993745 · MKJ Automated External Defibrillators (non-wearable) · Cardiovascular
Feb 2000 90d
K-DEFIB/PACE RADIOLUCENT ADULT ELECTRODE, MODEL KRT-60
K991007 · MKJ Automated External Defibrillators (non-wearable) · Cardiovascular
Aug 1999 150d
K-DEFIB/PACE ADULT ELECTRODE MODEL NUMBER KDP-60
K981737 · MKJ Automated External Defibrillators (non-wearable) · Cardiovascular
Dec 1998 205d
K-DEFIB/PACE PEDIATRIC ELECTRODE
K954504 · MKJ Automated External Defibrillators (non-wearable) · Cardiovascular
Nov 1995 50d
K-DEFIB/PACE PEDIATRIC ELECTRODE
K934692 · MKJ Automated External Defibrillators (non-wearable) · Cardiovascular
Jan 1995 481d
K-KLIP
K940801 · DRX Electrode, Electrocardiograph · Cardiovascular
Aug 1994 162d
PEDIATRIC DEFIB K-PADS
K935083 · LDD Dc-defibrillator, Low-energy, (including Paddles) · Cardiovascular
Jul 1994 273d
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