FDA 510(k) Application Details - K042689

Device Classification Name	Radioimmunoassay, Cortisol   More FDA Info for this Device
510(K) Number	K042689
Device Name	Radioimmunoassay, Cortisol
Applicant	NICHOLS INSTITUTE DIAGNOSTICS 1311 CALLE BATIDO SAN CLEMENTE, CA 92673 US Other 510(k) Applications for this Company
Contact	JIMMY WONG Other 510(k) Applications for this Contact
Regulation Number	862.1205   More FDA Info for this Regulation Number
Classification Product Code	CGR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/29/2004
Decision Date	12/09/2004
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