FDA 510(k) Applications Submitted by Cordis US Corp.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| 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. |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact