FDA 510(k) Application Details - K042291

Device Classification Name	Electrode, Ion Specific, Potassium   More FDA Info for this Device
510(K) Number	K042291
Device Name	Electrode, Ion Specific, Potassium
Applicant	BECKMAN COULTER, INC. 200 SOUTH KRAEMER BLVD.,W-104 P.O. BOX 8000 BREA, CA 92822-8000 US Other 510(k) Applications for this Company
Contact	MARY BETH TANG Other 510(k) Applications for this Contact
Regulation Number	862.1600   More FDA Info for this Regulation Number
Classification Product Code	CEM Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/24/2004
Decision Date	11/12/2004
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