FDA 510(k) Application Details - K132353

Device Classification Name	More FDA Info for this Device
510(K) Number	K132353
Device Name	SUCTION LIPOPLASTY ACCESSORIES
Applicant	INEX ZA LA GOBETTE 60540 PUISEUX LE HAUBERGER PUISEUX LE HAUBERGER 60540 FR Other 510(k) Applications for this Company
Contact	RAYMOND PATEL Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	QPB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/29/2013
Decision Date	07/30/2014
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