Medical device makerLabelled 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 15, 2026, FDA's public records list CD Medical, Inc. with 11 510(k) clearances. The most recent is a 510(k) clearance dated Mar 30, 1994: CD HOME DIALYSERVICE HEMODIALYSIS TRAY.
| Mar 30, 1994 | CD HOME DIALYSERVICE HEMODIALYSIS TRAYK925654 · KOC | 510(k) clearances |
| Apr 9, 1991 | DRAKE WILLOCK SYSTEM 1000 DIALYSATE DELIVERY SYSTK910215 · FKP | 510(k) clearances |
| Jun 26, 1990 | WURTZ CHOLEY CLIP (TM)K901520 · GBZ | 510(k) clearances |
| Nov 8, 1989 | DRAKE WILLOCK REVERSE OSMOSIS WATER TREATMENT SYSTK894106 · FIP | 510(k) clearances |
| Dec 8, 1988 | ULTRX(TM) 850 ARTIFICIAL KIDNEYK884353 · KDI | 510(k) clearances |
| Apr 13, 1988 | 480 HIGH-FLOW ULTRAFILTRATION CONTROL DIALYSATEK880459 · FKP | 510(k) clearances |
| Oct 23, 1987 | 8810 PUMP-PUMP SINGLE NEEDLE DEVICEK873279 · FIF | 510(k) clearances |
| Jan 20, 1987 | SERAFLO(TM) BLOODLINES FOR HEMODIALYSISK864784 · FJK | 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
