The following data is part of a premarket notification filed by Grandway Technology (shenzhen) Limited with the FDA for Digital Automatic Blood Pressure Monitor Md2300.
| Device ID | K143735 |
| 510k Number | K143735 |
| Device Name: | Digital Automatic Blood Pressure Monitor MD2300 |
| Classification | System, Measurement, Blood-pressure, Non-invasive |
| Applicant | Grandway Technology (Shenzhen) Limited Block 6 And 7, Zhu Keng Industrial Zone, Ping Shan, Long Gang District, Shenzhen, CN 518118 |
| Contact | Patrick Chow |
| Correspondent | Patrick Chow Grandway Technology (Shenzhen) Limited Block 6 And 7, Zhu Keng Industrial Zone, Ping Shan, Long Gang District, Shenzhen, CN 518118 |
| Product Code | DXN |
| CFR Regulation Number | 870.1130 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-12-30 |
| Decision Date | 2015-07-23 |
| Summary: | summary |