Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Zeus Technologies — 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) |
|---|---|---|---|---|---|
| K840012 | INDIRECT FLUORESCENT ANTIBODY MYCO | Zeus Technologies | 1984-02-27 | 54 | 0 |
| K831026 | INDIRECT FLUORESCENT ANTIBODY REAGENTS | Zeus Technologies | 1983-06-22 | 84 | 0 |
| K830783 | VERI-STAPH | Zeus Technologies | 1983-04-08 | 28 | 0 |
| K822859 | DIRECT FA CONJUGATE FOR LEGIONELLA SPP | Zeus Technologies | 1983-02-16 | 142 | 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