FDA 510(k) Application Details - K013992

Device Classification Name	Radioimmunoassay, Parathyroid Hormone   More FDA Info for this Device
510(K) Number	K013992
Device Name	Radioimmunoassay, Parathyroid Hormone
Applicant	NICHOLS INSTITUTE DIAGNOSTICS 33051 CALLE AVIADOR SAN JUAN CAPISTRANO, CA 92675 US Other 510(k) Applications for this Company
Contact	ROBERT SCHMIDT 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	12/04/2001
Decision Date	12/13/2001
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	Y
Expedited Review