Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
The Anthros Medical Group — Predicate Candidate Screening
2 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K933060 | S-610 & 2-628 WHEELED SHOWER STRETCHERS | The Anthros Medical Group | 1994-02-04 | 227 | 0 |
| K921752 | AMBULATOR | The Anthros Medical Group | 1992-05-04 | 21 | 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