The following data is part of a premarket notification filed by Asahi Intecc Co., Ltd. with the FDA for Asahi Ptca Guide Wire Confianza Pro.
Device ID | K041531 |
510k Number | K041531 |
Device Name: | ASAHI PTCA GUIDE WIRE CONFIANZA PRO |
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 | 2004-06-08 |
Decision Date | 2004-08-03 |
Summary: | summary |