Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Medi-Man Rehabilitation 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) |
|---|---|---|---|---|---|
| K992779 | A-2000 BATHING SYSTEMS; HYDROSONIC BATHIN SYSTEM | Medi-Man Rehabilitation Products, Inc. | 2000-01-13 | 148 | 0 |
| K925195 | MALIBU BATHING SYSTEM | Medi-Man Rehabilitation Products, Inc. | 1994-10-17 | 732 | 0 |
| K924905 | MEDI-PLINTH | Medi-Man Rehabilitation Products, Inc. | 1993-02-16 | 140 | 0 |
| K844976 | MEDI-MAN WATER POWERED BATH LIFT & HYDRAULIC LIFT | Medi-Man Rehabilitation Products, Inc. | 1985-04-01 | 96 | 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