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 BrukerLabelled 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 Bruker Medical Imaging, Inc. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Mar 13, 1992: MODIFIED MAGNETIC RESONANCE IMAGING SYTEM MOD. R28.
| Mar 13, 1992 | MODIFIED MAGNETIC RESONANCE IMAGING SYTEM MOD. R28K915657 · LNH | 510(k) clearances |
| Nov 29, 1991 | MAG RES IMAG SYST/BRUKER MODEL R28 WHOLE BODY SCANK913463 · LNH | 510(k) clearances |
| Nov 13, 1990 | BRUKER R-28,HEAD AND CHEST ANGIOGRAPHY IMAGING ADDK903661 · LNH | 510(k) clearances |
| Apr 30, 1990 | BRUKER R28 WHOLE-BODY MR SCANNERK900026 · LNH | 510(k) clearances |
| Mar 9, 1990 | MAGNETIC RESONANCE SYSTEM MODEL BMT-1100K895328 · LNH | 510(k) clearances |
| Nov 15, 1989 | 1989 SOFTWARE REVISION TO THE BMT-1100K894714 · LNH | 510(k) clearances |
| Jun 23, 1989 | MAGNETIC RESONANCE SYSTEM, MODEL BMT 1100,MODIFIEDK891760 · LNH | 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
