EEG Electrode Template— 510(k) K191225
Substantially EquivalentRhythmlink International, LLC
FDA 510(k) clearance K191225 for EEG Electrode Template, Substantially Equivalent on 2019-08-05. Applicant: Rhythmlink International, LLC.
Clearance details
- Applicant
- Rhythmlink International, LLC
- Product code
- Code GXY
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Columbia, SC, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.