FDA 510(k) Application Details - K071517

Device Classification Name	Container, Sharps   More FDA Info for this Device
510(K) Number	K071517
Device Name	Container, Sharps
Applicant	A.B.M. ITALIA S.P.A VIA LNG. G. TALIERCIO, 1 RONCADELLE DI ORMELLE 31024 IT Other 510(k) Applications for this Company
Contact	FRANCO GRAVA Other 510(k) Applications for this Contact
Regulation Number	880.5570   More FDA Info for this Regulation Number
Classification Product Code	MMK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/04/2007
Decision Date	04/02/2008
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review