The following data is part of a premarket notification filed by Grandway Technology (shenzhen) Limited with the FDA for Digital Automatic Blood Pressure Monitor Md36 Series.
Device ID | K191593 |
510k Number | K191593 |
Device Name: | Digital Automatic Blood Pressure Monitor MD36 Series |
Classification | System, Measurement, Blood-pressure, Non-invasive |
Applicant | Grandway Technology (Shenzhen) Limited no. 5, 2nd Industrial Zone, Zhukeng Community, Longtian Street, Pingshan District Shenzhen, CN 518118 |
Contact | Patrick Chow |
Correspondent | Patrick Chow Grandway Technology (Shenzhen) Limited no. 5, 2nd Industrial Zone, Zhukeng Community, Longtian Street, Pingshan District Shenzhen, CN 518118 |
Product Code | DXN |
CFR Regulation Number | 870.1130 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2019-06-14 |
Decision Date | 2019-07-22 |
Summary: | summary |