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 13, 2026, FDA's public records list Resonex with 21 510(k) clearances. The most recent is a 510(k) clearance dated Mar 21, 1994: FAST SPIN ECHO (FSE).
| Date | Record | Source |
|---|---|---|
| Mar 21, 1994 | FAST SPIN ECHO (FSE)K935369 · LNH | 510(k) clearances |
| Mar 16, 1994 | NOISE FILTER FOR PARADIGM MAGNETIC RESONANCE IMAGING SYSTEMK935570 · LNH | 510(k) clearances |
| Nov 2, 1993 | ECG GATING UNITK931392 · LNH | 510(k) clearances |
| Jan 12, 1993 | 3DTOF MRAK923870 · LNH | 510(k) clearances |
| Nov 23, 1992 | KINEMATIC MRI MOVIEMAKERK924154 · LNH | 510(k) clearances |
| Oct 30, 1992 | 3D IMAGINGK923823 · LNH | 510(k) clearances |
| Sep 4, 1992 | MAGNETIZATION TRANSFER CONTRASTK922677 · LNH | 510(k) clearances |
| Jun 22, 1992 | COILS FOR RX4000 & RX5000 MRI SYSTEMSK920254 · 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
