EV1000 Clinical Platform NI, EV1000 Clinical Platform
FDA 510(k) clearance K192058 · decided 2019-08-30
Clearance details
- K-number
- K192058
- Device name
- EV1000 Clinical Platform NI, EV1000 Clinical Platform
- Applicant
- Edwards Lifesciences, LLC
- Decision
- Substantially Equivalent
- Date received
- 2019-08-01
- Decision date
- 2019-08-30
- Days to decision
- 29 days
- Clearance type
- Special
- Product code
- DXN
- Device class
- 2
- Regulation number
- 870.1130
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Irvine, CA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.