Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
All-Pro Imaging Corp. — 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) |
|---|---|---|---|---|---|
| K001314 | MEDSCOPE | All-Pro Imaging Corp. | 2000-07-25 | 90 | 0 |
| K001321 | ALL-PRO 2010 | All-Pro Imaging Corp. | 2000-05-16 | 20 | 0 |
| K991435 | AII-PRO 100 PLUS AND ALL-PRO 200 | All-Pro Imaging Corp. | 1999-05-20 | 24 | 0 |
| K911291 | ALL-PRO 100 | All-Pro Imaging Corp. | 1991-07-03 | 100 | 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