FDA 510(k) Application Details - K955336

Device Classification Name	Device, Anti-Snoring   More FDA Info for this Device
510(K) Number	K955336
Device Name	Device, Anti-Snoring
Applicant	SCOTT FELDMAN DDS & NORMAN SHAPIRO DDS 6319 DESOTO AVE. SUITE 401 WOODLAND HILLS, CA 91367 US Other 510(k) Applications for this Company
Contact	SCOTT E FELDMAN 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	11/20/1995
Decision Date	01/04/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review