Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Preferred Medical Products — Predicate Candidate Screening
6 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
252 daysmedian FDA review time
445 days90th percentile
6clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K941153 | EPI-SPINAL ANESTHESIA TRAY | Preferred Medical Products | 1995-05-30 | 445 | 1 |
| K924699 | PMP MUSCLE STIMULATOR | Preferred Medical Products | 1993-04-30 | 225 | 0 |
| K920808 | OB/GYN DRAPE | Preferred Medical Products | 1993-02-19 | 364 | 0 |
| K904440 | LOCAL PLEXUS BLOCK ANESTHESIA CATHETER KITS | Preferred Medical Products | 1991-06-07 | 252 | 7 |
| K885278 | EPIDURAL ANESTHESIA TRAY | Preferred Medical Products | 1989-03-16 | 83 | 0 |
| K885277 | SPINAL ANESTHESIA TRAY | Preferred Medical Products | 1989-03-06 | 73 | 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