Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Microlife Intellectual Property GmbH, Switzerland · 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) |
|---|---|---|---|---|---|
| K151869 | Microlife Upper Arm Automatic Digital Blood Pressure Monitor | Microlife Intellectual Property GmbH, Switzerland | 2015-09-02 | 55 | 0 |
| K151330 | Microlife Wrist Watch Blood Pressure Monitor | Microlife Intellectual Property GmbH, Switzerland | 2015-07-14 | 56 | 0 |
| K140572 | MICROLIFE UPPER ARM AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR | Microlife Intellectual Property GmbH, Switzerland | 2014-07-02 | 118 | 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