FDA 510(k) Application Details - K060256

Device Classification Name	Hexokinase, Glucose   More FDA Info for this Device
510(K) Number	K060256
Device Name	Hexokinase, Glucose
Applicant	BECKMAN COULTER, INC. 200 S. KRAEMER BLVD. BREA, CA 92622 US Other 510(k) Applications for this Company
Contact	MARY BETH TANG Other 510(k) Applications for this Contact
Regulation Number	862.1345   More FDA Info for this Regulation Number
Classification Product Code	CFR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/01/2006
Decision Date	02/27/2006
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
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