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 C.G.H. Medical with 11 510(k) clearances. The most recent is a 510(k) clearance dated May 12, 1995: COBE CENTRYSYSTEM CS500 DIALYZER.
| May 12, 1995 | COBE CENTRYSYSTEM CS500 DIALYZERK941708 · FJI | 510(k) clearances |
| Jan 25, 1995 | GAMBRO POLYFLUX II HEMODIALYZERIALYZER HEMODIAFILTERK933818 · KDI | 510(k) clearances |
| Sep 30, 1994 | CENTRYSYSTEM 3 WITH CHARTS/BP OPTIONK925522 · KOC | 510(k) clearances |
| Aug 5, 1994 | FILTRAL HEMODIALYZERSK920757 · KDI | 510(k) clearances |
| Jul 7, 1994 | LUNDIA ALPHA 700 HEMODIALYZERK931720 · KDI | 510(k) clearances |
| Jun 27, 1994 | HEMOSPAL KIT B22 / MULTIFLOW 60 KITK924437 · KDI | 510(k) clearances |
| Mar 22, 1994 | GAMBRO BICART 720GK940601 · KPO | 510(k) clearances |
| May 27, 1992 | GAMBRO ENGSTROM Y FILTER PKG. ALONE W/ VAR.MODELSK915154 · CAN | 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
