FDA 510(k) Application Details - K021409

Device Classification Name	Radioimmunoassay, Luteinizing Hormone   More FDA Info for this Device
510(K) Number	K021409
Device Name	Radioimmunoassay, Luteinizing Hormone
Applicant	PHAMATECH INC. 9530 PADGETT ST., #101-106 SAN DIEGO, CA 92126 US Other 510(k) Applications for this Company
Contact	CARL A MONGIOVI Other 510(k) Applications for this Contact
Regulation Number	862.1485   More FDA Info for this Regulation Number
Classification Product Code	CEP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/03/2002
Decision Date	05/24/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CH - Clinical Chemistry
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review