FDA 510(k) Application Details - K993096

Device Classification Name	Enzymatic Esterase--Oxidase, Cholesterol   More FDA Info for this Device
510(K) Number	K993096
Device Name	Enzymatic Esterase--Oxidase, Cholesterol
Applicant	LIFESTREAM TECHNOLOGIES, INC. 51O CLEARWATER LOOP, SUITE 101 POST FALLS, ID 83854 US Other 510(k) Applications for this Company
Contact	JACKSON B CONNOLLY Other 510(k) Applications for this Contact
Regulation Number	862.1175   More FDA Info for this Regulation Number
Classification Product Code	CHH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/28/1999
Decision Date	12/20/1999
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