FDA 510(k) Application Details - K932661

Device Classification Name	More FDA Info for this Device
510(K) Number	K932661
Device Name	WHATMAN BODY FLUID COLLECTION PAPER:WHATMAN BFC180
Applicant	WHATMAN SPECIALTY PRODUCTS, INC. 6 JUST RD. FAIRFIELD, NJ 07004 US Other 510(k) Applications for this Company
Contact	RICHARD J COPPOLA Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	PJC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/02/1993
Decision Date	04/17/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CH - Clinical Chemistry
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review