FDA 510(k) Application Details - K130341

Device Classification Name	More FDA Info for this Device
510(K) Number	K130341
Device Name	STRAWBERRY, STRAWBERRY & CREAM
Applicant	LASER LIPO LIMITED HEATH HOUSE, CROCKHAM HILL EDENBRIDGE, KENT TN8 6ST GB Other 510(k) Applications for this Company
Contact	Ian Cobley Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	OLI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/11/2013
Decision Date	09/06/2013
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review