Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Electronic Monitors, 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) |
|---|---|---|---|---|---|
| K922393 | EMITENS ELECTRODES | Electronic Monitors, Inc. | 1993-07-21 | 427 | 0 |
| K842696 | LIFE-MASK INFANT RESUSCITATOR | Electronic Monitors, Inc. | 1984-07-27 | 16 | 0 |
| K822319 | RE1000 HEART RATE MONITOR | Electronic Monitors, Inc. | 1982-09-14 | 42 | 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