Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Aea Srl — 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) |
|---|---|---|---|---|---|
| K203674 | B Dispensing Line | Aea Srl | 2021-09-27 | 285 | 0 |
| K192770 | S dispensing line | Aea Srl | 2020-12-17 | 444 | 0 |
| K132011 | APOTECA DUG COMPOUNDING DOSING DEVICE,APOTECA I.V. TRANSFER | Aea Srl | 2014-03-21 | 263 | 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