Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Rifton Equipment For the Handicapped · Predicate Candidate Screening
7 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
26 daysmedian FDA review time
34 days90th percentile
7clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K921894 | RIFTON MOBILE PRONE STANDERS | Rifton Equipment For the Handicapped | 1992-05-26 | 34 | 0 |
| K921817 | RIFTON MOR219 19 & RIFTON MOR225 25 | Rifton Equipment For the Handicapped | 1992-04-29 | 14 | 0 |
| K921272 | ACTIVITY CHAIR | Rifton Equipment For the Handicapped | 1992-04-07 | 21 | 0 |
| K892697 | E653 OBLONG ABDUCTION BLOCK | Rifton Equipment For the Handicapped | 1989-05-09 | 26 | 0 |
| K892698 | E655 ADJUSTABLE ABDUCTION BLOCK W/HIP STABILIZER | Rifton Equipment For the Handicapped | 1989-05-09 | 26 | 0 |
| K892699 | E613 PAIR OF SUPPORT BLOCKS | Rifton Equipment For the Handicapped | 1989-05-09 | 26 | 0 |
| K892700 | E65 35 PRONE STANDER | Rifton Equipment For the Handicapped | 1989-05-09 | 26 | 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