Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Merck KGaALabelled by claude-sonnet-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record. See the Merck KGaA group view.
As of Nov 15, 2026, FDA's public records list Amicon with 20 510(k) clearances. The most recent is a 510(k) clearance dated Aug 5, 1993: CENTRICON -50 CONCENTRATOR.
| Aug 5, 1993 | CENTRICON -50 CONCENTRATORK930168 · JJH | 510(k) clearances |
| Nov 1, 1990 | AMICON DIAFILTER 30 HEMOCONCENTRATORK902837 · KDI | 510(k) clearances |
| May 18, 1990 | AMICON HEMOCONCENTRATOR SETK901286 · KDI | 510(k) clearances |
| Feb 16, 1990 | CENTRIPREP 100K900280 · JJP | 510(k) clearances |
| Jan 11, 1990 | AMICON MINIFILTER PLUS HEMOFILTERK895405 · KDI | 510(k) clearances |
| Jul 20, 1989 | CENTRICON CONCENTRATORK893733 · JJH | 510(k) clearances |
| Jun 13, 1989 | AMICON VITAFIBER FLO-PATH BIORECT/VLS CELL CULT SYK892645 · KJF | 510(k) clearances |
| Feb 19, 1988 | AMICON EQUALINE FLUID BALANCE SYSTEMK875121 · KPF | 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
