Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
U. S. A. Imaging 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) |
|---|---|---|---|---|---|
| K813177 | US ALOKA SSD-256 ULTRASONIC SCANNER | U. S. A. Imaging Corp. | 1982-03-05 | 113 | 0 |
| K813397 | SSD-240 ULTRASONIC SCANNER | U. S. A. Imaging Corp. | 1982-03-02 | 88 | 0 |
| K813398 | SSD-203 ULTRASONIC SCANNER | U. S. A. Imaging Corp. | 1982-03-01 | 87 | 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