Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Omron Marshall Products, 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) |
|---|---|---|---|---|---|
| K903133 | OMRON OSCILLOMETRIC DIGITAL BP MONITOR-HEM-405C | Omron Marshall Products, Inc. | 1991-01-18 | 185 | 0 |
| K903134 | OMRON AUTO OSCILLOMETRIC DIG BP MONT/HEM-704C 705C | Omron Marshall Products, Inc. | 1991-01-08 | 175 | 0 |
| K901963 | OMRON TRAVEL TOOTHBRUSH, MODEL HT-B02 | Omron Marshall Products, Inc. | 1990-06-26 | 56 | 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