Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Electrical Geodesics, Incorporated — 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) |
|---|---|---|---|---|---|
| K063797 | GEODESIC EEG SYSTEM 300 | Electrical Geodesics, Incorporated | 2007-01-25 | 34 | 0 |
| K043309 | GEODESIC PHOTOGRAMMETRY SYSTEM | Electrical Geodesics, Incorporated | 2005-01-26 | 56 | 0 |
| K033399 | GEODESIC EEG SYSTEM SERIES 100 | Electrical Geodesics, Incorporated | 2004-08-04 | 285 | 0 |
| K012079 | GEODESIC EEG SYSTEM, MODEL 200 | Electrical Geodesics, Incorporated | 2001-09-19 | 78 | 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