FDA 510(k) Application Details - K101709

Device Classification Name	Device, Anti-Snoring   More FDA Info for this Device
510(K) Number	K101709
Device Name	Device, Anti-Snoring
Applicant	STEVEN B. LAMBERG, DDS 800 E. LEIGH STREET SUITE 206-5 RICHMOND, VA 23219 US Other 510(k) Applications for this Company
Contact	EMILY B ROSSITER 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	06/17/2010
Decision Date	08/18/2010
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