Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Rehab Technology, 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) |
|---|---|---|---|---|---|
| K921084 | THE EXCELSIOR | Rehab Technology, Inc. | 1992-04-07 | 32 | 0 |
| K850313 | TELEVISION CONTROL OPTION 1219 | Rehab Technology, Inc. | 1985-04-25 | 90 | 0 |
| K850314 | TELEVISION CONTROL OPTION 1220 | Rehab Technology, Inc. | 1985-04-25 | 90 | 0 |
| K840808 | ECU 1218 | Rehab Technology, Inc. | 1984-03-19 | 24 | 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