ASAHI PTCA Guide Wires, ASAHI Corsair Microcatheter, ASAHI Corsair Pro Microcatheter— 510(k) K171933
Substantially EquivalentAsahi Intecc Co., Ltd.
FDA 510(k) clearance K171933 for ASAHI PTCA Guide Wires, ASAHI Corsair Microcatheter, ASAHI Corsair Pro Microcatheter, Substantially Equivalent on 2018-02-12. Applicant: Asahi Intecc Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Asahi Intecc Co., Ltd.
- Product code
- Code DQX
- Device class
- Class 2
- Regulation
- 21 CFR 870.1330
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Hagoya-Shi, JP
Recent devices under product code DQX
view allMore clearances from Asahi Intecc Co., Ltd.
view allAdverse events under product code DQX
product code DQX- Death
- 298
- Injury
- 4,385
- Malfunction
- 7,203
- Other
- 5
- Total
- 11,891
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.