Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Panasonic Corporation (Panasonic) · Predicate Candidate Screening
2 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K981431 | PANASONIC WRIST BLOOD PRESSURE METER, MODEL EW280 | Panasonic Corporation (Panasonic) | 1999-03-03 | 317 | 0 |
| K981542 | PANASONIC WRIST BLOOD PRESSURE METER, MODEL EW284 | Panasonic Corporation (Panasonic) | 1999-03-03 | 308 | 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