Grandway Technology (Shenzhen) Limited - FDA 510(k) Cleared Devices
Recent clearances: Digital Automatic Blood Pressure Monitor MD36 Series, Digital Automatic Wrist Blood Pressure Monitor MD4300, Digital Automatic Blood Pressure Monitor BPM41 Series, Digital Automatic Blood Pressure Monitor BPM45 Series
21
Total
21
Cleared
0
Denied
FDA 510(k) Regulatory Record - Grandway Technology (Shenzhen) Limited Cardiovascular ✕
21 devices
Cleared
Jul 22, 2019
Digital Automatic Blood Pressure Monitor MD36 Series
Cardiovascular
38d
Cleared
Apr 10, 2018
Digital Automatic Wrist Blood Pressure Monitor MD4300
Cardiovascular
334d
Cleared
Jul 07, 2017
Digital Automatic Blood Pressure Monitor BPM41 Series, Digital Automatic...
Cardiovascular
196d
Cleared
Jun 07, 2017
Digital Automatic Blood Pressure Monitor MD3600
Cardiovascular
162d
Cleared
Jan 19, 2017
Digital Automatic Wrist Blood Pressure Monitor SWBPM22 Series
Cardiovascular
73d
Cleared
Sep 29, 2015
Digital Automatic Blood Pressure Monitor BPM30 and BPM31 Series
Cardiovascular
29d
Cleared
Aug 07, 2015
Digital Automatic Wrist Blood Pressure Monitor MD3900
Cardiovascular
57d
Cleared
Aug 07, 2015
Digital Automatic Wrist Blood Pressure Monitor MD3200
Cardiovascular
57d
Cleared
Jul 23, 2015
Digital Automatic Blood Pressure Monitor MD2300
Cardiovascular
205d
Cleared
Jun 11, 2015
Digital Automatic Blood Pressure Monitor BPM25 & BPM26 Series [Model No.:...
Cardiovascular
118d
Cleared
May 02, 2015
Digital Automatic Blood Pressure Monitor BPM28 Series - MD2800, MD2810
Cardiovascular
123d
Cleared
Apr 03, 2015
Digital Automatic Wrist Blood Pressure Monitor MD2400
Cardiovascular
94d