FDA 510(k) Application Details - K974818

Device Classification Name	Immunoassay Method, Troponin Subunit   More FDA Info for this Device
510(K) Number	K974818
Device Name	Immunoassay Method, Troponin Subunit
Applicant	RADIOMETER AMERICA, INC. 810 SHARON DR. WESTLAKE, OH 44145-1598 US Other 510(k) Applications for this Company
Contact	DONALD L BAKER Other 510(k) Applications for this Contact
Regulation Number	862.1215   More FDA Info for this Regulation Number
Classification Product Code	MMI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/23/1997
Decision Date	01/16/1998
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