Medical device makerLabelled 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 Bayer. FDA records under its name, each linked to the record. See the Bayer group view.
As of Nov 14, 2026, FDA's public records list Bayer Agfa Division with 3 510(k) clearances. The most recent is a 510(k) clearance dated Apr 30, 1998: CP 1000, CURIX HT 330, CLASSIC E.O.S., CURIX HT 530, MAMORAY HT 300, MAMORAY CMPACT PLUS….
| Apr 30, 1998 | CP 1000, CURIX HT 330, CLASSIC E.O.S., CURIX HT 530, MAMORAY HT 300, MAMORAY CMPACT PLUS, CURIX COMPACT PLUS, CURIX COMSK981280 · IXW | 510(k) clearances |
| Mar 9, 1998 | ADC COMPACT (AGFA DIAGNOSTIC CENTER)K974597 · KPR | 510(k) clearances |
| Jan 27, 1997 | LR 5200 LASER FILM RECORDERK964414 · LMC | 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
