FDA 510(k) Application Details - K033083

Device Classification Name	Reagent, Borrelia Serological Reagent   More FDA Info for this Device
510(K) Number	K033083
Device Name	Reagent, Borrelia Serological Reagent
Applicant	TRINITY BIOTECH USA P.O. BOX 1059 JAMESTOWN, NY 14702-1059 US Other 510(k) Applications for this Company
Contact	Bonnie B DeJoy Other 510(k) Applications for this Contact
Regulation Number	866.3830   More FDA Info for this Regulation Number
Classification Product Code	LSR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/29/2003
Decision Date	11/26/2003
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