FDA 510(k) Application Details - K063232

Device Classification Name	Radioimmunoassay, Parathyroid Hormone   More FDA Info for this Device
510(K) Number	K063232
Device Name	Radioimmunoassay, Parathyroid Hormone
Applicant	BIOKIT S.A. CAN MALE LLISSA D'AMUNT BARCELONA 08186 ES Other 510(k) Applications for this Company
Contact	JOAN GUIXER Other 510(k) Applications for this Contact
Regulation Number	862.1545   More FDA Info for this Regulation Number
Classification Product Code	CEW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/25/2006
Decision Date	06/19/2007
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