Invivo Corporation (Business Trade Name: Philips) 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
dS Breast Coil 7ch 1.5T510(k)Oct 3, 2023Radiology	Radiology	510(k)Substantially Equivalent (Special)	Oct 3, 2023
8ch Wrist Coil510(k)Aug 31, 2022Radiology	Radiology	510(k)Substantially Equivalent (Traditional)	Aug 31, 2022
1.5 T/R Quad Extremity Coil, 1.5T 8CH T/R Knee Coil510(k)Aug 23, 2022Radiology	Radiology	510(k)Substantially Equivalent (Traditional)	Aug 23, 2022
dS Sentinelle Breast 16ch 1.5T Coil510(k)Aug 8, 2022Radiology	Radiology	510(k)Substantially Equivalent (Traditional)	Aug 8, 2022
dS Sentinelle Breast 16ch 3.0T Coil510(k)Aug 8, 2022Radiology	Radiology	510(k)Substantially Equivalent (Traditional)	Aug 8, 2022
ds Head 32ch 3.0T510(k)Oct 29, 2021Radiology	Radiology	510(k)Substantially Equivalent (Traditional)	Oct 29, 2021