FDA 510(k) Application Details - K992127

Device Classification Name	Immunoassay Method, Troponin Subunit   More FDA Info for this Device
510(K) Number	K992127
Device Name	Immunoassay Method, Troponin Subunit
Applicant	SPECTRAL DIAGNOSTICS, INC. 5550 N.W. 102 PLACE MIAMI, FL 33178 US Other 510(k) Applications for this Company
Contact	FRANCEE S BOCHES 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	06/23/1999
Decision Date	10/04/1999
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