EKOS+ Endovascular Device— 510(k) K220866
Substantially EquivalentBoston Scientific
FDA 510(k) clearance K220866 for EKOS+ Endovascular Device, Substantially Equivalent on 2022-04-20. Applicant: Boston Scientific.
Clearance details
- Applicant
- Boston Scientific
- Product code
- Code QEY
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Maple Grove, MN, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.