Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Toitu of America, Inc. · 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) |
|---|---|---|---|---|---|
| K894036 | TOITU FETAL ACTOCARDIOGRAPH, MT-332 | Toitu of America, Inc. | 1989-11-06 | 153 | 0 |
| K890139 | TOITU DOPPLER FETUS DETECTOR, FD-400D | Toitu of America, Inc. | 1989-03-29 | 75 | 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