Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Accuimage Diagnostics 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) |
|---|---|---|---|---|---|
| K024149 | PRIMELUNG | Accuimage Diagnostics Corp. | 2003-02-21 | 67 | 0 |
| K012106 | ACCUIMAGE SMARTGATE UPGRADE | Accuimage Diagnostics Corp. | 2001-09-25 | 81 | 0 |
| K990241 | ACCUIMAGE, ACCUVIEW DIAGNOSTIC IMAGING, WORKSTATION W/ACCUSC | Accuimage Diagnostics Corp. | 1999-09-23 | 241 | 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