FDA 510(k) Application Details - K024339

Device Classification Name	Cholinesterase Test Paper   More FDA Info for this Device
510(K) Number	K024339
Device Name	Cholinesterase Test Paper
Applicant	COZART BIOSCIENCE LTD. 45 MILTON PARK ABINGDON OXFORDSHIRE OX14 4RU OX14 4RU GB Other 510(k) Applications for this Company
Contact	ROBERTO LIDDI Other 510(k) Applications for this Contact
Regulation Number	862.3240   More FDA Info for this Regulation Number
Classification Product Code	DIG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/27/2002
Decision Date	04/07/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	TX - Clinical Toxicology
Review Advisory Committee	TX - Clinical Toxicology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review