FDA 510(k) Application Details - K122154

Device Classification Name	Massager, Powered Inflatable Tube   More FDA Info for this Device
510(K) Number	K122154
Device Name	Massager, Powered Inflatable Tube
Applicant	FIG, LLC 2839 HARVEST MOON DRIVE ORANGE PARK, FL 32073 US Other 510(k) Applications for this Company
Contact	JOE ADKINS Other 510(k) Applications for this Contact
Regulation Number	890.5650   More FDA Info for this Regulation Number
Classification Product Code	IRP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/20/2012
Decision Date	11/21/2012
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	PM - Physical Medicine
Review Advisory Committee	PM - Physical Medicine
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review