FDA 510(k) Application Details - K960993

Device Classification Name	Microfilter, Blood Transfusion   More FDA Info for this Device
510(K) Number	K960993
Device Name	Microfilter, Blood Transfusion
Applicant	PALL BIOMEDICAL PRODUCTS CO. 2200 NORTHERN BLVD. EAST HILLS, NY 11548 US Other 510(k) Applications for this Company
Contact	ROBERT A DICKSTEIN, PH.D. Other 510(k) Applications for this Contact
Regulation Number	880.5440   More FDA Info for this Regulation Number
Classification Product Code	CAK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/12/1996
Decision Date	04/22/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review