FDA 510(k) Applications Submitted by KVIKNA EHF
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K143487 | 12/08/2014 | Lifelines iEEG | KVIKNA EHF |
| K123665 | 11/28/2012 | LIFELINES IEEG | KVIKNA EHF |
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