Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Advanced Rehabilitative Technology, Inc. · Predicate Candidate Screening
3 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K915369 | THE EQUALIZER | Advanced Rehabilitative Technology, Inc. | 1993-03-22 | 481 | 0 |
| K912328 | ELECTRONIC MUSCLE STIMULATORS, EXCEL II, MODIFIED | Advanced Rehabilitative Technology, Inc. | 1992-11-06 | 532 | 0 |
| K903711 | RHEOLOGIC I | Advanced Rehabilitative Technology, Inc. | 1991-01-16 | 155 | 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