Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in SwedenLabelled 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 Elema AB with 63 510(k) clearances. The most recent is a 510(k) clearance dated Sep 5, 2003: COMPRESSOR MINI, 115 V, MODEL 64 81 779 EH81E.
| Sep 5, 2003 | COMPRESSOR MINI, 115 V, MODEL 64 81 779 EH81EK023354 · BTI | 510(k) clearances |
| Jan 23, 2002 | KION ANAESTHESIA SYSTEM, MODEL 65 03 879 E392EK010923 · MHX | 510(k) clearances |
| Dec 18, 2001 | SERVOI VENTILATOR SYSTEM, MODEL 64 87 800 E407EK010925 · CBK | 510(k) clearances |
| Oct 5, 2000 | CATHCOR DESKTOPK002137 · DQK | 510(k) clearances |
| May 26, 2000 | MODIFICATION TO KION ANESTHESIA SYSTEMK001315 · BSZ | 510(k) clearances |
| Oct 14, 1997 | SERVO VENTILATOR 300AK970839 · CBK | 510(k) clearances |
| Oct 25, 1996 | SIEMENS SERVO SCREEN 390 AND SERVO COMPUTER MODULE 990K960168 · CBK | 510(k) clearances |
| Oct 25, 1996 | SERVO VENTILATOR 300 COMPUTER INTERFACEK960010 · CBK | 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
