Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Progressive Medical Technology, Inc. · Predicate Candidate Screening
5 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
56 daysmedian FDA review time
238 days90th percentile
5clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K923710 | OSCILLAIR 3000 LOW AIR LOSS KINETIC THERAPY BED | Progressive Medical Technology, Inc. | 1993-03-22 | 238 | 0 |
| K915092 | TALLEY TM300 SEQUENTIAL MULTICOM COMPRESSION SYST | Progressive Medical Technology, Inc. | 1992-02-11 | 82 | 0 |
| K915637 | TALLEY TM500 SEQUENTIAL MULTICOM COMPRESSION SYST. | Progressive Medical Technology, Inc. | 1992-02-11 | 56 | 0 |
| K915638 | TALLEY TM200 INTERMTTENT COMPRESSION UNIT | Progressive Medical Technology, Inc. | 1992-02-11 | 56 | 0 |
| K915671 | B.A.S.E. BELLOWS AIR SUPPORT EQUIPMENT | Progressive Medical Technology, Inc. | 1992-01-13 | 49 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda