FDA 510(k) Application Details - K093710

Device Classification Name	Device, Anti-Snoring   More FDA Info for this Device
510(K) Number	K093710
Device Name	Device, Anti-Snoring
Applicant	ALLEN J. MOSES, DDS, LTD. 233 S. WACKER DR. CHICAGO, IL 60606 US Other 510(k) Applications for this Company
Contact	ALLEN J MOSES 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	12/02/2009
Decision Date	05/12/2010
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Statement
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review