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 15, 2026, FDA's public records list Progressive Medical Technology, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Mar 22, 1993: OSCILLAIR 3000 LOW AIR LOSS KINETIC THERAPY BED.
| Mar 22, 1993 | OSCILLAIR 3000 LOW AIR LOSS KINETIC THERAPY BEDK923710 · IKZ | 510(k) clearances |
| Feb 11, 1992 | TALLEY TM200 INTERMTTENT COMPRESSION UNITK915638 · IRP | 510(k) clearances |
| Feb 11, 1992 | TALLEY TM500 SEQUENTIAL MULTICOM COMPRESSION SYST.K915637 · IRP | 510(k) clearances |
| Feb 11, 1992 | TALLEY TM300 SEQUENTIAL MULTICOM COMPRESSION SYSTK915092 · IRP | 510(k) clearances |
| Jan 13, 1992 | B.A.S.E. BELLOWS AIR SUPPORT EQUIPMENTK915671 · IOQ | 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
