Meridian AG 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
MR Q; MR Q SUPINE; MR Q SLT510(k)Jan 25, 2024Ophthalmic	Ophthalmic	510(k)Substantially Equivalent (Traditional)	Jan 25, 2024
Merilas 532 shortpulse, Merilas 577 shortpulse, Merilas 810 shortpulse510(k)Sep 12, 2023Ophthalmic	Ophthalmic	510(k)Substantially Equivalent (Traditional)	Sep 12, 2023