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 |