Beijing Choice Electronic Technology Co., Ltd. FDA Approvals

0 new drug approvals and 8 device clearances on file. This applicant is not matched to a listed company.

Newest first

A new drug approval is an original application; a 510(k) is a device shown equivalent to one already sold.

Product	What it is	Route	Decided
Pulse Oximeter (MD300C228)510(k)Jun 21, 2024Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Jun 21, 2024
Wrist Pulse Oximeter510(k)Nov 30, 2023Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Nov 30, 2023
Pulse Oximeter510(k)Aug 12, 2023Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Aug 12, 2023
Pulse Oximeter510(k)Mar 8, 2023Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Mar 8, 2023
Electronic Pulse Stimulator510(k)Oct 21, 2022Neurology	Neurology	510(k)Substantially Equivalent (Traditional)	Oct 21, 2022
Pulse Oximeter510(k)Feb 11, 2022Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Feb 11, 2022
Infrared Thermometer510(k)Jan 21, 2022General Hospital	General Hospital	510(k)Substantially Equivalent (Traditional)	Jan 21, 2022
Vital Signs Monitor510(k)Nov 15, 2021Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Nov 15, 2021