FDA 510(k) Application Details - K172111

Device Classification Name	More FDA Info for this Device
510(K) Number	K172111
Device Name	Vevazz LED
Applicant	Vevazz, LLC 3839 McKinney Ave. #251 Dallas, TX 75204 US Other 510(k) Applications for this Company
Contact	Jamie Fettig Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	OLI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/13/2017
Decision Date	11/22/2017
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review