Kvikna Ehf is one of 18943 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kvikna Ehf - FDA 510(k) Cleared Devices
Recent clearances: Lifelines iEEG, LIFELINES IEEG
2
Total
2
Cleared
0
Denied
Kvikna Ehf has 2 FDA 510(k) cleared medical devices. Based in Crofton, US.
Historical record: 2 cleared submissions from 2013 to 2015. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Kvikna Ehf Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Smith Assoicates as regulatory consultant.
FDA 510(k) Regulatory Record - Kvikna Ehf
2 devices