The following data is part of a premarket notification filed by Shenzhen Pump Medical System Co., Ltd. with the FDA for Arm Automatic Blood Pressure Monitor.
Device ID | K151258 |
510k Number | K151258 |
Device Name: | Arm Automatic Blood Pressure Monitor |
Classification | System, Measurement, Blood-pressure, Non-invasive |
Applicant | SHENZHEN PUMP MEDICAL SYSTEM CO., LTD. 2/F WEST, M-7 SINOSTEEL BUILDING, MAQUELING ESTATE HI-TECH INDUSTRIAL PARK Nanshan District, Shenzhen, Guangdong, CN 518057 |
Contact | Xie Qiongyu |
Correspondent | Migo Yang SHENZHEN PUMP MEDICAL SYSTEM CO., LTD. 2/F WEST, M-7 SINOSTEEL BUILDING, MAQUELING ESTATE HI-TECH INDUSTRIAL PARK Nanshan District, Shenzhen, Guangdong, CN 518057 |
Product Code | DXN |
CFR Regulation Number | 870.1130 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-05-12 |
Decision Date | 2016-02-18 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
06947679701194 | K151258 | 000 |