Pentaferte Italia S.R.L. 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
Pentaflush510(k)Jul 20, 2022General Hospital	General Hospital	510(k)Substantially Equivalent (Traditional)	Jul 20, 2022
ENFit enteral syringes (NUTRIFIT)510(k)Feb 28, 2022Gastroenterology, Urology	Gastroenterology, Urology	510(k)Substantially Equivalent (Traditional)	Feb 28, 2022