ASAHI PTCA GUIDE WIRE
Wire, Guide, Catheter
ASAHI INTECC CO., LTD.
The following data is part of a premarket notification filed by Asahi Intecc Co., Ltd. with the FDA for Asahi Ptca Guide Wire.
Pre-market Notification Details
| Device ID | K052339 |
| 510k Number | K052339 |
| Device Name: | ASAHI PTCA GUIDE WIRE |
| Classification | Wire, Guide, Catheter |
| Applicant | ASAHI INTECC CO., LTD. 1301 DOVE STREET, SUITE #350 Newport Beach, CA 92660 |
| Contact | Yoshi Terai |
| Correspondent | Yoshi Terai ASAHI INTECC CO., LTD. 1301 DOVE STREET, SUITE #350 Newport Beach, CA 92660 |
| Product Code | DQX |
| CFR Regulation Number | 870.1330 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2005-08-26 |
| Decision Date | 2005-11-30 |
| Summary: | summary |
Trademark Results [ASAHI PTCA GUIDE WIRE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ASAHI PTCA GUIDE WIRE 78248368 2844884 Dead/Cancelled |
Asahi Intecc Co., Ltd. 2003-05-12 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.