FDA 510(k) Application Details - K020694

Device Classification Name	Kit,Typing,Hla-Dqb   More FDA Info for this Device
510(K) Number	K020694
Device Name	Kit,Typing,Hla-Dqb
Applicant	CHESHIRE DIAGNOSTICS LTD. MANAGEMENT CENTRE, INWARD WAY ELLESMERE PORT CHESHIRE CH65 3EN GB Other 510(k) Applications for this Company
Contact	NEIL B STRINGER Other 510(k) Applications for this Contact
Regulation Number	866.5660   More FDA Info for this Regulation Number
Classification Product Code	MVS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/04/2002
Decision Date	04/19/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	IM - Immunology
Review Advisory Committee	IM - Immunology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review