FDA 510(k) Application Details - K060277

Device Classification Name	Apparatus, Suction, Ward Use, Portable, Ac-Powered   More FDA Info for this Device
510(K) Number	K060277
Device Name	Apparatus, Suction, Ward Use, Portable, Ac-Powered
Applicant	BOEHRINGER LABORATORIES 500 E. WASHINGTON ST. NORRISTOWN, PA 19401 US Other 510(k) Applications for this Company
Contact	CHRISTOPHER RADL Other 510(k) Applications for this Contact
Regulation Number	878.4780   More FDA Info for this Regulation Number
Classification Product Code	JCX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/02/2006
Decision Date	03/03/2006
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