FDA 510(k) Application Details - K022654

Device Classification Name	Colorimetric Method, Cpk Or Isoenzymes   More FDA Info for this Device
510(K) Number	K022654
Device Name	Colorimetric Method, Cpk Or Isoenzymes
Applicant	ROCHE DIAGNOSTICS CORP. 9115 HAGUE RD. PO BX 50457 INDIANAPOLIS, IN 46250-0457 US Other 510(k) Applications for this Company
Contact	SHERRI L COENEN Other 510(k) Applications for this Contact
Regulation Number	862.1215   More FDA Info for this Regulation Number
Classification Product Code	JHY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/09/2002
Decision Date	08/29/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CH - Clinical Chemistry
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review