eego amplifiers— 510(k) K172312
Substantially EquivalentEemagine Medical Imaging Solutions GmbH
FDA 510(k) clearance K172312 for eego amplifiers, Substantially Equivalent on 2018-03-30. Applicant: Eemagine Medical Imaging Solutions GmbH.
Clearance details
- Applicant
- Eemagine Medical Imaging Solutions GmbH
- Product code
- Code GWL
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Berlin, DE
Data sourced from openFDA. This site is unofficial and independent of the FDA.