510(k) K133618 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
DIGITAL AUTOMATIC WRIST BLOOD PRESSURE MONITOR WBPM22 SERIES
| Applicant | Grandway Technology (Shenzhen) Limited, Shenshen, Guang Dong, CN |
| Decision | Substantially Equivalent, Mar 5, 2014 |
| Received | Nov 25, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133618
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.