The following data is part of a premarket notification filed by Orantech Inc. with the FDA for Reusable Nibp Cuff.
Device ID | K173197 |
510k Number | K173197 |
Device Name: | Reusable NIBP Cuff |
Classification | Blood Pressure Cuff |
Applicant | Orantech Inc. Zone#A, 4F, 1st Bld, 7th Industrial Zone Yulv Community, GongMing Guangming New District, Shenzhen, CN 518106 |
Contact | Yunxi Xiong |
Correspondent | Kevin Wang Chonconn Medical Device Consulting Co., Ltd. 22A, Haijing Square, No. 18, Taizi Road Nanshan District, Shenzhen, CN 518067 |
Product Code | DXQ |
CFR Regulation Number | 870.1120 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-10-02 |
Decision Date | 2018-08-21 |
Summary: | summary |