Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Median Technologies · 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) |
|---|---|---|---|---|---|
| K251474 | Median LCS (internal name) / eyonis LCS (trade name) (1.0) | Median Technologies | 2026-02-06 | 269 | 0 |
| K071241 | LMS-LIVER | Median Technologies | 2007-06-08 | 36 | 0 |
| K070868 | LMS-LUNG/TRACK | Median Technologies | 2007-05-15 | 47 | 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