FirmLabelled 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., part of Merck KGaALabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record. See the Merck KGaA group view.
As of Nov 15, 2026, FDA's public records list Millipore with 32 510(k) clearances. The most recent is a 510(k) clearance dated Mar 12, 2010: LIGHT DIAGNOSTICS HUMAN METAPNEUMOVIRUS DFA KIT, MODEL CATALOG NUMBER 3124.
| Mar 12, 2010 | LIGHT DIAGNOSTICS HUMAN METAPNEUMOVIRUS DFA KIT, MODEL CATALOG NUMBER 3124K093815 · OMG | 510(k) clearances |
| Apr 1, 2009 | LIGHT DIAGNOSTICS HSV 1/2 TYPING DFA KITK081527 · GQL | 510(k) clearances |
| Jan 17, 2003 | MILLEX VV, GV, AND HV SYRINGE FILTER UNITSK023892 · BSN | 510(k) clearances |
| Apr 4, 2002 | MILLEX GP STERILIZING FILTER UNIT, MODEL SLGP 033 RK013988 · BSN | 510(k) clearances |
| Jun 10, 1997 | MILLEX - MP FILTER UNIT (SLMPO25SS/SLMPL25SS)K963717 · BSN | 510(k) clearances |
| May 27, 1994 | ULTRAFREE-CLK941326 · JJH | 510(k) clearances |
| Apr 21, 1994 | MILLEX, DUALEX (PLUS, ULTRA)K934069 · FIB | 510(k) clearances |
| Dec 11, 1992 | WATERS(TM) 996 PDAK924347 · KIE | 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
