FDA 510(k) Application Details - K120261

Device Classification Name	Set, Administration, Intravascular   More FDA Info for this Device
510(K) Number	K120261
Device Name	Set, Administration, Intravascular
Applicant	Perouse Medical Route du Manoir Ivry-le-Temple FRANCE 60173 FR Other 510(k) Applications for this Company
Contact	Isabelle Jeanty Other 510(k) Applications for this Contact
Regulation Number	880.5440   More FDA Info for this Regulation Number
Classification Product Code	FPA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/27/2012
Decision Date	05/02/2012
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review