Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Dytek Corp. — 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) |
|---|---|---|---|---|---|
| K781245 | LUNG EXER. BAG, POST-OP, MODIFIED | Dytek Corp. | 1978-09-20 | 65 | 0 |
| K760168 | PENCIL, ELECTROSURGICAL | Dytek Corp. | 1976-08-09 | 34 | 0 |
| K760167 | BAG, POST OPERATIVE LUNG EXERCIZING BLOW | Dytek Corp. | 1976-08-06 | 31 | 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