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. Device class: 2.
Clearance details
- Applicant
- Boston Scientific
- Product code
- Code QEY
- Device class
- Class 2
- Regulation
- 21 CFR 870.5150
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Maple Grove, MN, US
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More clearances from Boston Scientific
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