FDA 510(k) Application Details - K971886

Device Classification Name	Radioimmunoassay, Human Chorionic Gonadotropin   More FDA Info for this Device
510(K) Number	K971886
Device Name	Radioimmunoassay, Human Chorionic Gonadotropin
Applicant	UNOTECH DIAGNOSTICS, INC. 2235 POLVOROSA AVE., SUITE 220 SAN LEANDRO, CA 94577 US Other 510(k) Applications for this Company
Contact	KEN WU Other 510(k) Applications for this Contact
Regulation Number	862.1155   More FDA Info for this Regulation Number
Classification Product Code	JHI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/22/1997
Decision Date	06/11/1997
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