Eko Model E5 System (EME5), Eko DUO— 510(k) K170874
Substantially EquivalentEko Devices, Inc.
FDA 510(k) clearance K170874 for Eko Model E5 System (EME5), Eko DUO, Substantially Equivalent on 2017-05-19. Applicant: Eko Devices, Inc..
Clearance details
- Applicant
- Eko Devices, Inc.
- Product code
- Code DQD
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Berkeley, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.