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 |