The following data is part of a premarket notification filed by Shenzhen Urion Technology Co.,ltd with the FDA for U80 Series Upper Arm Electronic Blood Pressure Monitor.
Device ID | K160019 |
510k Number | K160019 |
Device Name: | U80 Series Upper Arm Electronic Blood Pressure Monitor |
Classification | System, Measurement, Blood-pressure, Non-invasive |
Applicant | SHENZHEN URION TECHNOLOGY CO.,LTD 4TH BUILDING, HI-TECH INDUSTRIAL ZONE, HEPING COMMUNITY, FUYONG STREET, BAOAN Shenzhen, CN 518103 |
Contact | Autumn Liu |
Correspondent | Autumn Liu SHENZHEN URION TECHNOLOGY CO.,LTD 4TH BUILDING, HI-TECH INDUSTRIAL ZONE, HEPING COMMUNITY, FUYONG STREET, BAOAN Shenzhen, CN 518103 |
Product Code | DXN |
CFR Regulation Number | 870.1130 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-01-05 |
Decision Date | 2016-04-22 |
Summary: | summary |