The following data is part of a premarket notification filed by Kaneka Corporation with the FDA for Metacross Rx Pta Balloon Dilitation Catheter.
Device ID | K150865 |
510k Number | K150865 |
Device Name: | Metacross RX PTA Balloon Dilitation Catheter |
Classification | Catheter, Percutaneous |
Applicant | Kaneka Corporation 1-12-32, Akasaka, Minato-ku Tokyo, JP |
Contact | Toshihiko Motomine |
Correspondent | Christopher M Sloan Quintiles Consulting 1801 Rockville Pike, Suite 300 Rockville, MD 20852 |
Product Code | DQY |
CFR Regulation Number | 870.1250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-04-01 |
Decision Date | 2015-08-03 |
Summary: | summary |