Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Micro Focus Imaging, Inc. — 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) |
|---|---|---|---|---|---|
| K953404 | OSTEO-RAY 100 | Micro Focus Imaging, Inc. | 1995-11-30 | 133 | 0 |
| K953292 | CP 100/30 | Micro-Focus Imaging., Inc. | 1995-11-22 | 132 | 0 |
| K926434 | SIS-300(N)-DIA SCAN | Micro-Focus Imaging., Inc. | 1993-03-18 | 85 | 0 |
| K852634 | MICRO-FOCUS 50 CABINET X-RAY | Micro-Focus Imaging., Inc. | 1985-07-19 | 29 | 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