FDA 510(k) Application Details - DEN210012

Device Classification Name	More FDA Info for this Device
510(K) Number	DEN210012
Device Name	vPatch
Applicant	Virility Medical 24 Hanagar St., Suite 106 Hod-Hasharon 4527713 IL Other 510(k) Applications for this Company
Contact	Bosmat Friedman Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	QRC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/30/2021
Decision Date	11/23/2021
Decision	DENG -
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status
Type	Direct
Reviewed By Third Party	N
Expedited Review