FDA 510(k) Application Details - K160531

Device Classification Name	Device, Anti-Snoring   More FDA Info for this Device
510(K) Number	K160531
Device Name	Device, Anti-Snoring
Applicant	FIRMA INGEMARSSON VILVORDEVEJ 61 CHARLOTTENLUND 2920 DK Other 510(k) Applications for this Company
Contact	Natashia Ingemarsson-Matzen Other 510(k) Applications for this Contact
Regulation Number	872.5570   More FDA Info for this Regulation Number
Classification Product Code	LRK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/25/2016
Decision Date	09/01/2016
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review