Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Akers Laboratories, 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) |
|---|---|---|---|---|---|
| K040293 | HEALTHTEST HEPARIN/PLATELET FACTOR 4 ANTIBODY ASSAY | Akers Laboratories, Inc. | 2004-05-28 | 112 | 0 |
| K031579 | INSTAREAD LITHIUM SYSTEM | Akers Laboratories, Inc. | 2003-12-19 | 213 | 0 |
| K030815 | AKERS LABORATORIES INC. BLOOD CELL SEPARATOR | Akers Laboratories, Inc. | 2003-09-17 | 187 | 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