Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Vail Products, Inc. — Predicate Candidate Screening
4 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K982783 | VAIL 1000 ENCLOSED BED | Vail Products, Inc. | 1998-10-05 | 59 | 1 |
| K963622 | VAIL 2000 ENCLOSED BED | Vail Products, Inc. | 1997-05-07 | 239 | 1 |
| K963589 | VAIL 3000 BED ENCLOSURE | Vail Products, Inc. | 1997-04-21 | 224 | 0 |
| K963210 | VAIL 100 PEDIATRIC CRIB | Vail Products, Inc. | 1996-11-13 | 89 | 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