K231478 is an FDA 510(k) clearance for the Digital Blood Pressure Monitor (Model: YB-800). This device is classified as a System, Measurement, Blood-pressure, Non-invasive (Class II - Special Controls, product code DXN).
Submitted by Wenzhou Yosun Medical Technology Co.,Ltd (Wenzhou, CN). The FDA issued a Cleared decision on December 15, 2023, 207 days after receiving the submission on May 22, 2023.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.1130.
| 510(k) Number | K231478 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 22, 2023 |
| Decision Date | December 15, 2023 |
| Days to Decision | 207 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 |