FDA 510(k) Application Details - K990814

Device Classification Name	Plasma, Coagulation Factor Deficient   More FDA Info for this Device
510(K) Number	K990814
Device Name	Plasma, Coagulation Factor Deficient
Applicant	PRECISION BIOLOGIC 900 WINDMILL RD., SUITE 100 DARTMOUTH, N.S. B3B 1P7 CA Other 510(k) Applications for this Company
Contact	SANDY MORRISON Other 510(k) Applications for this Contact
Regulation Number	864.7290   More FDA Info for this Regulation Number
Classification Product Code	GJT Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/11/1999
Decision Date	06/07/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HE - Hematology
Review Advisory Committee	HE - Hematology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review