FDA 510(k) Applications Submitted by Cordis US Corp.

FDA 510(k) Number Submission Date Device Name Applicant
K233637 11/13/2023 Cordis BRITECROSS Support Catheter Cordis US Corp.
K221832 06/23/2022 SABER .014 PTA Dilatation Catheter; SABERX .014 PTA Dilatation Catheter Cordis US Corp.
K230704 03/14/2023 RAIN SheathÖ Tibial Pedal Introducer Cordis US Corp.
K232573 08/25/2023 INFINITIÖ Ambi Angiographic Catheter Cordis US Corp.


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