FDA 510(k) Application Details - K092903

Device Classification Name	Pump, Portable, Aspiration (Manual Or Powered)   More FDA Info for this Device
510(K) Number	K092903
Device Name	Pump, Portable, Aspiration (Manual Or Powered)
Applicant	MAQUET GMBH AND CO. KG KEHLER STRASSE 31 RASTATT 76437 DE Other 510(k) Applications for this Company
Contact	ANNETTE JAKOB Other 510(k) Applications for this Contact
Regulation Number	878.4780   More FDA Info for this Regulation Number
Classification Product Code	BTA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/21/2009
Decision Date	12/01/2009
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	Y
Expedited Review