FDA 510(k) Application Details - K200125

Device Classification Name	Mouthguard, Prescription   More FDA Info for this Device
510(K) Number	K200125
Device Name	Mouthguard, Prescription
Applicant	Erkodent Erich Kopp GmbH Siemensstrasse 3 Pfalzgrafenweiler 72285 DE Other 510(k) Applications for this Company
Contact	Hans-Peter Kopp 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	01/21/2020
Decision Date	10/28/2020
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