Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Ohio Imaging, Inc. — 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) |
|---|---|---|---|---|---|
| K945261 | PRISM 1500XP NUCLEAR GAMMA CAMERA SYSTEM | Ohio Imaging, Inc. | 1995-03-21 | 144 | 0 |
| K934722 | PRISM 3000 NUCLEAR GAMMA CAMERA SYSTEM MODIFICATION | Ohio Imaging, Inc. | 1994-05-13 | 226 | 0 |
| K882312 | MODEL 3000 NUCLEAR CAMERA | Ohio Imaging, Inc. | 1988-07-14 | 41 | 1 |
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