Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Dyna Corp. — Predicate Candidate Screening
5 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
56 daysmedian FDA review time
69 days90th percentile
5clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K972528 | DYNA GLIDE 2600 ROLL-IN AMBULANCE COT (95759) | Dyna Corp. | 1997-07-28 | 21 | 0 |
| K962181 | HARE MODEL 2000 EZ LOADER MODEL 95555 | Dyna Corp. | 1996-08-01 | 56 | 0 |
| K902503 | HARE FOLDING BACK EMERGENCY STRETCHER | Dyna Corp. | 1990-06-26 | 21 | 0 |
| K900670 | HARE EMERGENCY STRETCHER | Dyna Corp. | 1990-04-23 | 69 | 0 |
| K900671 | HARE EMERGENCY STRETCHER WITH WHEELS | Dyna Corp. | 1990-04-23 | 69 | 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