Murata Vios, Inc. 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
Vios Monitoring System(TM) Model 2050; Vios Central Station Monitor/Vios Central Server Software 2050510(k)Jan 23, 2025Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Jan 23, 2025
Vios Monitoring System(TM) Model 2050; Vios Central Station Monitor/Vios Central Server Software510(k)Mar 22, 2024Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Mar 22, 2024