Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Katecho with 26 510(k) clearances. The most recent is a 510(k) clearance dated Oct 12, 2001: K-DEFIB/PACE ADULT ELECTRODE, MODEL KDP-85.
| Date | Record | Source |
|---|---|---|
| Oct 12, 2001 | K-DEFIB/PACE ADULT ELECTRODE, MODEL KDP-85K012404 · DRO | 510(k) clearances |
| May 23, 2001 | KM-30 TENS ELECTRODEK010543 · GXY | 510(k) clearances |
| Dec 14, 2000 | K-DEFIB/PACE MULTIFUCTION PEDIATRIC ELECTRODE, MODEL KDP-70AK003228 · MKJ | 510(k) clearances |
| Nov 21, 2000 | K-DEFIB/PACE, MODEL KDP-60AK002806 · MKJ | 510(k) clearances |
| Nov 7, 2000 | KM-10 TENS ELECTRODEK000870 · GXY | 510(k) clearances |
| Feb 3, 2000 | K-DEFIB/PACE ADULT ELECTRODE, MODEL KDP-80K993745 · MKJ | 510(k) clearances |
| Aug 23, 1999 | K-DEFIB/PACE RADIOLUCENT ADULT ELECTRODE, MODEL KRT-60K991007 · MKJ | 510(k) clearances |
| Dec 9, 1998 | K-DEFIB/PACE ADULT ELECTRODE MODEL NUMBER KDP-60K981737 · MKJ | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
