Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in JapanLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Konica MinoltaLabelled 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 Konica Minolta Sensing with 3 510(k) clearances. The most recent is a 510(k) clearance dated May 11, 2006: KONICA MINOLTA PULSOX-300, 300I.
| May 11, 2006 | KONICA MINOLTA PULSOX-300, 300IK053419 · DQA | 510(k) clearances |
| Feb 12, 2003 | MINOLTA PULSOX-2K021469 · DQA | 510(k) clearances |
| Aug 2, 2001 | MINOLTA PULSOX-3SI, PULSOX-3IA, PULSOX-3LIK010413 · DQA | 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
