Digital Automatic Blood Pressure Monitor MD2300— 510(k) K143735

Clearance details

Applicant

Grandway Technology (Shenzhen) Limited

Product code

Code DXN

Device class

Class 2

Regulation

21 CFR 870.1130

Advisory panel

Cardiovascular

Date received

2014-12-30

Decision date

2015-07-23

Decision

Substantially Equivalent

Clearance type

Traditional

Location

Shenzhen, Guang Dong, CN

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• K163113 — Digital Automatic Wrist Blood Pressure Monitor SWBPM22 Series2017-01-19

Death

3

Injury

169

Malfunction

1,019

Other

2

Total

1,193

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →