Katecho, Inc.

Medical device manufacturer in Des Moines, IA.

26510(k) clearances
0PMA approvals
0recalls

Device types

510(k) clearances

510(k)DeviceDecision
K012404K-Defib/Pace Adult Electrode, Model KDP-85DRO · Traditional 10/12/2001SE
K010543KM-30 TENS ElectrodeGXY · Traditional 05/23/2001SE
K003228K-Defib/Pace Multifuction Pediatric Electrode, Model KDP-70AMKJ · Traditional 12/14/2000SE
K002806K-Defib/Pace, Model KDP-60AMKJ · Traditional 11/21/2000SE
K000870KM-10 TENS ElectrodeGXY · Traditional 11/07/2000SE
K993745K-Defib/Pace Adult Electrode, Model KDP-80MKJ · Traditional 02/03/2000SE
K991007K-Defib/Pace Radiolucent Adult Electrode, Model KRT-60MKJ · Traditional 08/23/1999SE
K981737K-Defib/Pace Adult Electrode Model Number KDP-60MKJ · Traditional 12/09/1998SE
K954504K-Defib/Pace Pediatric ElectrodeMKJ · Traditional 11/17/1995SE
K934692K-Defib/Pace Pediatric ElectrodeMKJ · Traditional 01/24/1995SE
K940801K-KlipDRX · Traditional 08/03/1994SE
K935083Pediatric Defib K-PadsLDD · Traditional 07/25/1994ST
K940586K-SnapDRX · Traditional 06/09/1994SE
K922202K-Stim ClearGZJ · Traditional 05/17/1993SE
K926175K-Defib/Pace Carbon ElectrodeDRO · Traditional 04/15/1993SE
K921679K-DisperseGZJ · Traditional 10/06/1992SE
K915328Gel-TacDRO · Traditional 06/29/1992SE
K914955K-Defib/Pace ElectrodeDRO · Traditional 05/14/1992SE
K913031K-StimGXY · Traditional 01/30/1992SE
K912381Low Back Strip (or) K-BackGZJ · Traditional 01/30/1992SE
K912587K-FreeLDD · Traditional 07/30/1991SE
K900997K-Sterile TENS ElectrodesGXY · Traditional 03/13/1990SE
K895662Defib K-PadsLDD · Traditional 01/18/1990SE
K863899K-Stik Defibrillation PadsLDD · Traditional 11/12/1986SE
K843829K-Mesh · Traditional 06/05/1985SE
K843557K-Apatite 20-40 Mesh K-Apatite 40-60ELE · Traditional 11/30/1984SE