Cordis Corporation FDA Approvals

0 new drug approvals and 4 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
ANGIOGUARD XP Emboli Capture Guidewire, ANGIOGUARD RX Emboli Capture Guidewire510(k)Apr 6, 2022Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Special)	Apr 6, 2022
SUPER TORQUE MB Angiographic Catheter with Radiopaque markerbands510(k)Feb 17, 2022Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Feb 17, 2022
SABER .035 Percutaneous Transluminal Angioplasty (PTA) Dilatation Catheter510(k)Apr 23, 2021Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Apr 23, 2021
Brite Tip Radianz Guiding Sheath510(k)Feb 26, 2021Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Feb 26, 2021