TrailBlazer Angled Support Catheter— 510(k) K162384
Substantially EquivalentMedtronic Vascular, Inc.(Formerly Ev3 Inc.)
FDA 510(k) clearance K162384 for TrailBlazer Angled Support Catheter, Substantially Equivalent on 2016-09-22. Applicant: Medtronic Vascular, Inc.(Formerly Ev3 Inc.).
Clearance details
- Applicant
- Medtronic Vascular, Inc.(Formerly Ev3 Inc.)
- Product code
- Code DQY
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Plymouth, MN, US
Adverse events under product code DQY
product code DQY- Death
- 464
- Injury
- 4,489
- Malfunction
- 13,721
- Other
- 2
- Total
- 18,676
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.