Mesi, Development of Medical Devices, Ltd.; Mesi D.O.O. 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
MESI mTablet ECG Diagnostic System, MESI mTablet ECG510(k)Jul 28, 2023Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Jul 28, 2023
MESI mTABLET TBI diagnostic system, MESI mTABLET TBI510(k)Apr 21, 2022Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Apr 21, 2022