The following data is part of a premarket notification filed by Ev3 Inc. with the FDA for Nanocorss .014 Otw Pta Dilatation Catheter.
Device ID | K082854 |
510k Number | K082854 |
Device Name: | NANOCORSS .014 OTW PTA DILATATION CATHETER |
Classification | Catheter, Percutaneous |
Applicant | EV3 INC. 4600 NATHAN LN. NORTH Plymouth, MN 55442 -2920 |
Contact | David Worrell |
Correspondent | David Worrell EV3 INC. 4600 NATHAN LN. NORTH Plymouth, MN 55442 -2920 |
Product Code | DQY |
CFR Regulation Number | 870.1250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2008-09-29 |
Decision Date | 2008-12-04 |