510(k) K163648 · DXN System, Measurement, Blood-Pressure, Non-Invasive

Digital Automatic Blood Pressure Monitor BPM41 Series, Digital Automatic Blood Pressure Monitor BPM45 Series

Applicant	Grandway Technology (Shenzhen) Limited, Shenzhen, CN
Decision	Substantially Equivalent, Jul 7, 2017
Received	Dec 23, 2016
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K163648

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.