FDA 510(k) Application Details - K001716

Device Classification Name	Apparatus, Suction, Ward Use, Portable, Ac-Powered   More FDA Info for this Device
510(K) Number	K001716
Device Name	Apparatus, Suction, Ward Use, Portable, Ac-Powered
Applicant	PFM PRODUKTE FUR DIE MEDIZIN AG 154 VIA LAMPARA RANCHO SANTA MARGARITA, CA 92688 US Other 510(k) Applications for this Company
Contact	SALVADORE F PALOMARES 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	06/05/2000
Decision Date	07/19/2000
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	N
Expedited Review