The following data is part of a premarket notification filed by Cordis Europa N.v. with the FDA for Cordis Powerflex Extreme Pta Balloon Catheter, Cordis Powerflex Plus Pta Balloon Catheter, Cordis Powerflex P3 Pta.
| Device ID | K032737 |
| 510k Number | K032737 |
| Device Name: | CORDIS POWERFLEX EXTREME PTA BALLOON CATHETER, CORDIS POWERFLEX PLUS PTA BALLOON CATHETER, CORDIS POWERFLEX P3 PTA |
| Classification | Catheter, Percutaneous |
| Applicant | CORDIS EUROPA N.V. 7 POWDER HORN DR. Warren, NJ 07059 |
| Contact | Karen Wilk |
| Correspondent | Karen Wilk CORDIS EUROPA N.V. 7 POWDER HORN DR. Warren, NJ 07059 |
| Product Code | DQY |
| CFR Regulation Number | 870.1250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-09-04 |
| Decision Date | 2003-10-02 |
| Summary: | summary |