Katecho, Inc.
Katecho, Inc. holds FDA 510(k) medical device clearances, first cleared 1984, most recent 2001.
Top product codes for Katecho, Inc.
Recent clearances by Katecho, Inc.
- K012404 — K-DEFIB/PACE ADULT ELECTRODE, MODEL KDP-85
- K010543 — KM-30 TENS ELECTRODE
- K003228 — K-DEFIB/PACE MULTIFUCTION PEDIATRIC ELECTRODE, MODEL KDP-70A
- K002806 — K-DEFIB/PACE, MODEL KDP-60A
- K000870 — KM-10 TENS ELECTRODE
- K993745 — K-DEFIB/PACE ADULT ELECTRODE, MODEL KDP-80
- K991007 — K-DEFIB/PACE RADIOLUCENT ADULT ELECTRODE, MODEL KRT-60
- K981737 — K-DEFIB/PACE ADULT ELECTRODE MODEL NUMBER KDP-60
- K954504 — K-DEFIB/PACE PEDIATRIC ELECTRODE
- K934692 — K-DEFIB/PACE PEDIATRIC ELECTRODE
- K940801 — K-KLIP
- K935083 — PEDIATRIC DEFIB K-PADS
- K940586 — K-SNAP
- K922202 — K-STIM CLEAR
- K926175 — K-DEFIB/PACE CARBON ELECTRODE
- K921679 — K-DISPERSE
- K915328 — GEL-TAC
- K914955 — K-DEFIB/PACE ELECTRODE
- K912381 — LOW BACK STRIP (OR) K-BACK
- K913031 — K-STIM
- K912587 — K-FREE
- K900997 — K-STERILE TENS ELECTRODES
- K895662 — DEFIB K-PADS
- K863899 — K-STIK DEFIBRILLATION PADS
- K843829 — K-MESH
- K843557 — K-APATITE 20-40 MESH K-APATITE 40-60
Data sourced from openFDA. This site is unofficial and independent of the FDA.