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

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

7 devices

1-7 of 7

Cleared May 23, 2001

KM-30 TENS ELECTRODE

Neurology · 89d

Cleared Nov 07, 2000

KM-10 TENS ELECTRODE

Neurology · 232d

Cleared May 17, 1993

Neurology · 371d

Cleared Oct 06, 1992

Neurology · 181d

Cleared Jan 30, 1992

LOW BACK STRIP (OR) K-BACK

Neurology · 246d

Cleared Jan 30, 1992

Neurology · 205d

Cleared Mar 13, 1990

K-STERILE TENS ELECTRODES

Neurology · 11d