Dia Imaging Analysis, 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
LVivo Software Application510(k)Mar 17, 2025Radiology	Radiology	510(k)Substantially Equivalent (Special)	Mar 17, 2025
LVivo Seamless510(k)Mar 6, 2025Radiology	Radiology	510(k)Substantially Equivalent (Special)	Mar 6, 2025
LVivo Software Application510(k)Mar 3, 2025Radiology	Radiology	510(k)Substantially Equivalent (Traditional)	Mar 3, 2025
LVivo Software Application510(k)Oct 4, 2024Radiology	Radiology	510(k)Substantially Equivalent (Special)	Oct 4, 2024
LVivo IQS510(k)May 24, 2024Radiology	Radiology	510(k)Substantially Equivalent (Special)	May 24, 2024
LVivo IQS510(k)Feb 1, 2023Radiology	Radiology	510(k)Substantially Equivalent (Traditional)	Feb 1, 2023
LVivo Seamless510(k)Dec 9, 2021Radiology	Radiology	510(k)Substantially Equivalent (Traditional)	Dec 9, 2021
LVivo Software Application510(k)Feb 5, 2021Radiology	Radiology	510(k)Substantially Equivalent (Special)	Feb 5, 2021