Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Ep Medical, Inc. — 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) |
|---|---|---|---|---|---|
| K935590 | EP MEDICAL, INC. EP-3 CLINICAL STIMULATOR | Ep Medical, Inc. | 1994-05-05 | 168 | 0 |
| K933069 | MODEL EP-2 CLINICAL STIMULATOR | Ep Medical, Inc. | 1993-10-21 | 121 | 0 |
| K901320 | ABSORBENT, DISPOSABLE URINARY DRAINAGE BAG | Ep Medical, Inc. | 1991-01-25 | 310 | 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