FDA 510(k) Application Details - K070327

Device Classification Name	Device, Anti-Snoring   More FDA Info for this Device
510(K) Number	K070327
Device Name	Device, Anti-Snoring
Applicant	SYBRON DENTAL SPECIALTIES, INC. 1717 WEST COLLINS AVE. ORANGE, CA 92867 US Other 510(k) Applications for this Company
Contact	COLLEEN BOSWELL 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	02/05/2007
Decision Date	05/25/2007
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review