Diagnostics makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Merck KGaA. 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 Serono Diagnostics with 25 510(k) clearances. The most recent is a 510(k) clearance dated Mar 11, 1996: SERIES 9100 PLUS AUTOMATED DIFFERENTIAL HEMATOLOGY ANALYZERS.
| Mar 11, 1996 | SERIES 9100 PLUS AUTOMATED DIFFERENTIAL HEMATOLOGY ANALYZERSK953598 · GKZ | 510(k) clearances |
| Jul 13, 1994 | SR1 DHEA-S ENZYME IMMUNOASSAYK942051 · JKC | 510(k) clearances |
| Sep 9, 1988 | T3 UPTAKE SEROZYME ENZYME IMMUNO KT/MAG SOLID PHASK883085 · KHQ | 510(k) clearances |
| Aug 8, 1988 | LH SEROZYME IMMUNOENZYMETRIC ASSAY KIT,MAG SOL PHAK882340 · CEP | 510(k) clearances |
| Mar 3, 1988 | T3 SEROZYME ENZYMEIMMUNOASSAY KIT, MAG SOLID PHASEK880388 · CDP | 510(k) clearances |
| Feb 11, 1988 | T4 SEROZYME ENZYMEIMMUNOASSAY KIT/MAG. SOLID PHASEK874866 · KLI | 510(k) clearances |
| Oct 20, 1987 | PROGESTERONE MAIA RADIOIMMUNO ASSAY KIT MAG SLD PHK873431 · JLS | 510(k) clearances |
| Sep 29, 1987 | LH MAIACLONE IMMUNORADIO. ASSAY KIT, MAG SOLID PHAK873186 · CEP | 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
