The following data is part of a premarket notification filed by Cordis Corp. with the FDA for Powerflex Pro Percutaneous Transluminal Angioplasty Catheter.
Device ID | K112797 |
510k Number | K112797 |
Device Name: | POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETER |
Classification | Catheter, Angioplasty, Peripheral, Transluminal |
Applicant | CORDIS CORP. 430 ROUTE 22 EAST Bridgewater, NJ 08807 |
Contact | Danna Marshall |
Correspondent | Danna Marshall CORDIS CORP. 430 ROUTE 22 EAST Bridgewater, NJ 08807 |
Product Code | LIT |
CFR Regulation Number | 870.1250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-09-26 |
Decision Date | 2012-05-04 |
Summary: | summary |