Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in IsraelLabelled 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 Biodan Medical Systems with 20 510(k) clearances. The most recent is a 510(k) clearance dated Sep 7, 1993: THYROID UPTAKE SYSTEM & ATOMLAB 950 MED. SPECTROME.
| Sep 7, 1993 | THYROID UPTAKE SYSTEM & ATOMLAB 950 MED. SPECTROMEK932153 · IZD | 510(k) clearances |
| May 26, 1993 | RTM REHABILITATION TREADMILL, MODEL #945-200K930261 · IOL | 510(k) clearances |
| Mar 29, 1993 | TREATMENT TABLE, MODEL #825-100K930262 · INO | 510(k) clearances |
| Mar 24, 1993 | TRACTION TABLE MODEL #825-200K930259 · JFB | 510(k) clearances |
| Feb 12, 1993 | NUCLEAR PATIENT SANNING TABLES, VARIOUS TYPESK926083 · IYX | 510(k) clearances |
| Dec 30, 1992 | CARDIAC STRESS TABLE, 056-180/UNIV ROLL STRESS ATTK926082 · IZI | 510(k) clearances |
| Nov 27, 1992 | UROLOGICAL C-ARM TABLE, MODEL #056-450K922591 · IXR | 510(k) clearances |
| Oct 20, 1992 | TRENDELENBURG ULTRASOUND TABLE, MODEL # 056-603K922605 · IYO | 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
