The following data is part of a premarket notification filed by Kaneka Corporation with the FDA for Otw Takeru Ptca Balloon Dilatation Catheter.
Device ID | K172264 |
510k Number | K172264 |
Device Name: | OTW Takeru PTCA Balloon Dilatation Catheter |
Classification | Catheters, Transluminal Coronary Angioplasty, Percutaneous |
Applicant | Kaneka Corporation 1-12-32, Akasaka, Minato-ku Tokyo, JP 107-6028 |
Contact | Toshihiko Motomine |
Correspondent | Christopher M. Sloan QuintilesIMS 1801 Rockville Pike, Suite 300 Rockville, MD 20852 |
Product Code | LOX |
CFR Regulation Number | 870.5100 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-07-27 |
Decision Date | 2018-03-19 |
Summary: | summary |