FDA 510(k) Application Details - K211856

Device Classification Name	More FDA Info for this Device
510(K) Number	K211856
Device Name	gammaCore Sapphire
Applicant	Electrocore, Inc. 200 Forge Way, Suite 205 Rockaway, NJ 07866 US Other 510(k) Applications for this Company
Contact	Mike Romaniw Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	PKR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/16/2021
Decision Date	09/10/2021
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review