The following data is part of a premarket notification filed by Kaneka Corporation with the FDA for Crosstella Rx Balloon Dilatation Catheter.
Device ID | K152873 |
510k Number | K152873 |
Device Name: | Crosstella RX Balloon Dilatation Catheter |
Classification | Catheter, Angioplasty, Peripheral, Transluminal |
Applicant | KANEKA CORPORATION 1-12-32, AKASAKA, MINATO-KU Tokyo, JP 107-6025 |
Contact | Toshihiko Motomine |
Correspondent | Christopher M Sloan QUINTILES CONSULTING 1801 ROCKVILLE PIKE, SUITE 300 Rockville, MD 20852 |
Product Code | LIT |
CFR Regulation Number | 870.1250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-09-30 |
Decision Date | 2016-01-22 |
Summary: | summary |