Electrocore, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Electrocore, LLC - FDA 510(k) Cleared Devices
Recent clearances: gammaCore Sapphire, gammaCore-S
4
Total
3
Cleared
1
Denied
Electrocore, LLC has 3 FDA 510(k) cleared medical devices. Based in Basking Ridge, US.
Historical record: 3 cleared submissions from 2017 to 2018. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Electrocore, LLC Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Electrocore, LLC
4 devices