Neurophet., Inc. FDA Approvals

0 new drug approvals and 6 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
Neurophet SCALE PET510(k)May 15, 2026Radiology	Radiology	510(k)Substantially Equivalent (Traditional)	May 15, 2026
Neurophet AQUA510(k)May 15, 2026Radiology	Radiology	510(k)Substantially Equivalent (Special)	May 15, 2026
Neurophet AQUA AD Plus510(k)Jan 29, 2026Radiology	Radiology	510(k)Substantially Equivalent (Traditional)	Jan 29, 2026
Neurophet AQUA (V3.1)510(k)Oct 25, 2024Radiology	Radiology	510(k)Substantially Equivalent (Traditional)	Oct 25, 2024
Neurophet AQUA510(k)May 10, 2023Radiology	Radiology	510(k)Substantially Equivalent (Traditional)	May 10, 2023
Neurophet SCALE PET510(k)Aug 5, 2022Radiology	Radiology	510(k)Substantially Equivalent (Traditional)	Aug 5, 2022