Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Ives Eeg Solutions, 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) |
|---|---|---|---|---|---|
| K071118 | GOLD CUP ELECTRODE, SILVER CUP ELECTRODE AND ELECTRODE WITH | Ives Eeg Solutions, Inc. | 2007-09-07 | 140 | 0 |
| K062880 | SUBDERMAL WIRE ELECTRODE, MODEL SWE | Ives Eeg Solutions, Inc. | 2006-12-22 | 87 | 0 |
| K060189 | PEDIATRIC SUBDERMAL WIRE ELECTRODE (PSWE) | Ives Eeg Solutions, Inc. | 2006-05-30 | 126 | 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