FDA 510(k) Application Details - K033747

Device Classification Name	Fluorometric Method, Cpk Or Isoenzymes   More FDA Info for this Device
510(K) Number	K033747
Device Name	Fluorometric Method, Cpk Or Isoenzymes
Applicant	RESPONSE BIOMEDICAL CORP. 8081 LOUGHEED HWY. BURNABY, BRITISH COLUMBIA V5A 1W9 CA Other 510(k) Applications for this Company
Contact	WILLIAM J RADVAK Other 510(k) Applications for this Contact
Regulation Number	862.1215   More FDA Info for this Regulation Number
Classification Product Code	JHX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/01/2003
Decision Date	05/17/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CH - Clinical Chemistry
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review