Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Monebo Technologies, 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) |
|---|---|---|---|---|---|
| K063044 | CARDIOBELT ELECTRODE BELT | Monebo Technologies, Inc. | 2007-03-23 | 170 | 0 |
| K062282 | MONEBO AUTOMATED ECG ANALYSIS AND INTERPRETATION SOFTWARE LI | Monebo Technologies, Inc. | 2007-03-22 | 227 | 0 |
| K043380 | MONEBO AUTOMATIC ARRHYTHMIA DETECTION SOFTWARE LIBRARY, VERS | Monebo Technologies, Inc. | 2005-04-26 | 139 | 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