FDA 510(k) Application Details - K000844

Device Classification Name	System, Test, Human Chorionic Gonadotropin   More FDA Info for this Device
510(K) Number	K000844
Device Name	System, Test, Human Chorionic Gonadotropin
Applicant	MIZUHO USA, INC. 6730 MESA RIDGE RD., SUITE D SAN DIEGO, CA 92121 US Other 510(k) Applications for this Company
Contact	BENEDICT ZIN Other 510(k) Applications for this Contact
Regulation Number	862.1155   More FDA Info for this Regulation Number
Classification Product Code	DHA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/15/2000
Decision Date	06/16/2000
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CH - Clinical Chemistry
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review