FDA 510(k) Application Details - K023836

Device Classification Name	Device, Anti-Snoring   More FDA Info for this Device
510(K) Number	K023836
Device Name	Device, Anti-Snoring
Applicant	STRONG DENTAL INC. 21525 RIDGETOP CIRCLE SUITE 320 STERLING, VA 20166 US Other 510(k) Applications for this Company
Contact	CLYDE A TAKEGUCHI 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	11/18/2002
Decision Date	07/08/2003
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