Medical device makerLabelled 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 14, 2026, FDA's public records list Bioview Ltd. with 5 510(k) clearances. The most recent is a 510(k) clearance dated May 9, 2014: DUET SYSTEM.
| May 9, 2014 | DUET SYSTEMK130775 · NTH | 510(k) clearances |
| Jan 23, 2007 | DUET SYSTEMK061602 · JOY | 510(k) clearances |
| Aug 16, 2005 | MODIFICATION TO DUET SYSTEMK050840 · JOY | 510(k) clearances |
| Sep 16, 2004 | DUET SYSTEMK040591 · JOY | 510(k) clearances |
| Aug 20, 2003 | DUET SYSTEMK030192 · JOY | 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
