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 SiemensLabelled 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 Siemens Medical Corp. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Sep 27, 2001: NUMARIS 4VA15A.
| Sep 27, 2001 | NUMARIS 4VA15AK012202 · LNH | 510(k) clearances |
| Mar 30, 2001 | AXIOM ARTIS MODULAR ANGIOGRAPHY SYSTEMK010721 · IZI | 510(k) clearances |
| Aug 10, 2000 | SIEMENS INTEGRATED OPERATING SYSTEM (SIOS)K994231 · ODA | 510(k) clearances |
| Jan 14, 2000 | MAGNETOM OPEN VIVA WITH PERMANENT MAGNETK994316 · LNH | 510(k) clearances |
| Mar 12, 1999 | 3D-ANGIOK984634 · JAK | 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
