FDA 510(k) Applications Submitted by BEIJING CHOICE ELECTRONIC TECHNOLOGY CO., LTD.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K220101 |
01/12/2022 |
Pulse Oximeter |
Beijing Choice Electronic Technology Co., Ltd. |
| K230172 |
01/20/2023 |
Pulse Oximeter |
Beijing Choice Electronic Technology Co., Ltd. |
| K211400 |
05/05/2021 |
Pulse Oximeter |
Beijing Choice Electronic Technology Co., Ltd. |
| K181503 |
06/07/2018 |
Fingertip Pulse Oximeter |
Beijing Choice Electronic Technology Co., Ltd. |
| K211752 |
06/07/2021 |
Infrared Thermometer |
Beijing Choice Electronic Technology Co., Ltd. |
| K211754 |
06/07/2021 |
Vital Signs Monitor |
Beijing Choice Electronic Technology Co., Ltd. |
| K221992 |
07/06/2022 |
Electronic Pulse Stimulator |
Beijing Choice Electronic Technology Co., Ltd. |
| K160268 |
02/02/2016 |
Fingertip Pulse Oximeter MD300CG11/MD300CG51 |
BEIJING CHOICE ELECTRONIC TECHNOLOGY CO., LTD. |
| K161560 |
06/06/2016 |
Fingertip Pulse Oximeter MD300CN310 |
BEIJING CHOICE ELECTRONIC TECHNOLOGY CO., LTD. |
| K162089 |
07/28/2016 |
Blood Pressure Monitor |
BEIJING CHOICE ELECTRONIC TECHNOLOGY CO., LTD. |
| K172366 |
08/04/2017 |
Wrist Pulse Oximeter |
Beijing Choice Electronic Technology Co., Ltd. |
| K152563 |
09/09/2015 |
Pulse Oximeter (MD300M/MD300K2) |
BEIJING CHOICE ELECTRONIC TECHNOLOGY CO., LTD. |
|
|
