FDA 510(k) Application Details - K974261

Device Classification Name	Antisera, If, Toxoplasma Gondii   More FDA Info for this Device
510(K) Number	K974261
Device Name	Antisera, If, Toxoplasma Gondii
Applicant	BOSTON BIOMEDICA, INC. 375 WEST ST. WEST BRIDGEWATER, MA 02379 US Other 510(k) Applications for this Company
Contact	PATRICIA E GARRETT Other 510(k) Applications for this Contact
Regulation Number	866.3780   More FDA Info for this Regulation Number
Classification Product Code	LJK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/13/1997
Decision Date	12/11/1997
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	MI - Microbiology
Review Advisory Committee	MI - Microbiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review