Medical Device Manufacturer · US , Des Moines , IA

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

26 submissions · 25 cleared · Since 1984

Total

Cleared

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.

Katecho, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Katecho, Inc.

26 devices

1-12 of 26

Cleared Oct 12, 2001

K-DEFIB/PACE ADULT ELECTRODE, MODEL KDP-85

K-DEFIB/PACE MULTIFUCTION PEDIATRIC ELECTRODE, MODEL KDP-70A

K003228 · MKJ

Cardiovascular · 59d

Cleared Nov 21, 2000

K-DEFIB/PACE, MODEL KDP-60A

K-DEFIB/PACE ADULT ELECTRODE, MODEL KDP-80

K993745 · MKJ

Cardiovascular · 90d

Cleared Aug 23, 1999

K-DEFIB/PACE RADIOLUCENT ADULT ELECTRODE, MODEL KRT-60

K991007 · MKJ

Cardiovascular · 150d

Cleared Dec 09, 1998

K-DEFIB/PACE ADULT ELECTRODE MODEL NUMBER KDP-60

K981737 · MKJ

Cardiovascular · 205d

Cleared Nov 17, 1995

K-DEFIB/PACE PEDIATRIC ELECTRODE

K954504 · MKJ

Cardiovascular · 50d

Cleared Jan 24, 1995

K-DEFIB/PACE PEDIATRIC ELECTRODE

K934692 · MKJ

Cardiovascular · 481d

Cleared Aug 03, 1994

K-KLIP

K940801 · DRX

Cardiovascular · 162d

Cleared Jul 25, 1994

PEDIATRIC DEFIB K-PADS

K935083 · LDD

Cardiovascular · 273d

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

FDA 510(k) Regulatory Record - Katecho, Inc.

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