Shenzhen Viatom Technology Co., Ltd. FDA Approvals

0 new drug approvals and 2 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 ( PO2, PO2A, PO2B)510(k)Feb 28, 2025Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Feb 28, 2025
Oxyfit Pulse Oximeter510(k)Nov 8, 2022Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Nov 8, 2022