K211288 is an FDA 510(k) clearance for the Microlife Wrist Watch Blood Pressure Monitor Model BP3GK1-4B. This device is classified as a System, Measurement, Blood-pressure, Non-invasive (Class II - Special Controls, product code DXN).
Submitted by Microlife Intellectual Property GmbH (Widnau, CH). The FDA issued a Cleared decision on November 4, 2021, 190 days after receiving the submission on April 28, 2021.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.1130.
| 510(k) Number | K211288 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 28, 2021 |
| Decision Date | November 04, 2021 |
| Days to Decision | 190 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | Summary PDF |
| Product Code | DXN — System, Measurement, Blood-pressure, Non-invasive |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.1130 |