The following data is part of a premarket notification filed by Sejoy Electronics & Instruments Co., Ltd. with the FDA for Arm-type Fully Automatic Digital Blood Pressure Monitor.
Device ID | K141755 |
510k Number | K141755 |
Device Name: | ARM-TYPE FULLY AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR |
Classification | System, Measurement, Blood-pressure, Non-invasive |
Applicant | SEJOY ELECTRONICS & INSTRUMENTS CO., LTD. BLDG 2, NO. 202, ZHENZHONG RD WEST LAKE ECONOMY & TECH ZONE Hangzhou, Zhejiang, CN 310030 |
Contact | Ren Yunhua |
Correspondent | Ren Yunhua SEJOY ELECTRONICS & INSTRUMENTS CO., LTD. BLDG 2, NO. 202, ZHENZHONG RD WEST LAKE ECONOMY & TECH ZONE Hangzhou, Zhejiang, CN 310030 |
Product Code | DXN |
CFR Regulation Number | 870.1130 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-06-30 |
Decision Date | 2014-11-19 |