FDA 510(k) Application Details - K033179

Device Classification Name	Pump, Portable, Aspiration (Manual Or Powered)   More FDA Info for this Device
510(K) Number	K033179
Device Name	Pump, Portable, Aspiration (Manual Or Powered)
Applicant	MEDELA AG LAETTICHSTRASSE 4 CH-6340 BAAR CH Other 510(k) Applications for this Company
Contact	WERNER FREI 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	10/01/2003
Decision Date	10/15/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	Y
Expedited Review