FDA 510(k) Application Details - K182820

Device Classification Name	Mouthguard, Prescription   More FDA Info for this Device
510(K) Number	K182820
Device Name	Mouthguard, Prescription
Applicant	Advanced Facialdontics LLC 325 Lake Ave. Unit 759 St. James, NY 11780 US Other 510(k) Applications for this Company
Contact	Scott Simonetti Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	MQC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/04/2018
Decision Date	07/17/2019
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review