FDA 510(k) Application Details - K021032

Device Classification Name	Radioimmunoassay, Acth   More FDA Info for this Device
510(K) Number	K021032
Device Name	Radioimmunoassay, Acth
Applicant	SCANTIBODIES LABORATORY, INC. 9336 ABRAHAM WAY SANTEE, CA 92071 US Other 510(k) Applications for this Company
Contact	RICHARD LENART Other 510(k) Applications for this Contact
Regulation Number	862.1025   More FDA Info for this Regulation Number
Classification Product Code	CKG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/29/2002
Decision Date	06/03/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CH - Clinical Chemistry
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review