Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Deltex Medical · Predicate Candidate Screening
3 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K052989 | DP240 240 HOUR DOPPLER PROBE | Deltex Medical | 2006-03-08 | 135 | 0 |
| K031706 | CARDIOQ, MODEL 9051-7005 | Deltex Medical | 2003-08-06 | 65 | 0 |
| K951369 | EDM | Deltex Medical | 1995-11-07 | 225 | 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