FDA 510(k) Application Details - K960412

Device Classification Name	Radioimmunoassay, Total Triiodothyronine   More FDA Info for this Device
510(K) Number	K960412
Device Name	Radioimmunoassay, Total Triiodothyronine
Applicant	BIOMERICA, INC. 1533 MONROVIA AVE. NEWPORT BEACH, CA 92663 US Other 510(k) Applications for this Company
Contact	JOSEPH IRANI Other 510(k) Applications for this Contact
Regulation Number	862.1710   More FDA Info for this Regulation Number
Classification Product Code	CDP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/29/1996
Decision Date	03/19/1996
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