510(k) K160349 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
Electronic Sphygmomanometer
| Applicant | Guangdong Biolight Meditech Co., Ltd., Zhuhai, CN |
| Decision | Substantially Equivalent, Nov 3, 2016 |
| Received | Feb 8, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160349
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.