FDA 510(k) Application Details - K014034

Device Classification Name	Ph Rate Measurement, Carbon-Dioxide   More FDA Info for this Device
510(K) Number	K014034
Device Name	Ph Rate Measurement, Carbon-Dioxide
Applicant	BECKMAN COULTER, INC. 200 SOUTH KRAEMER BLVD. W-110 BREA, CA 92822 US Other 510(k) Applications for this Company
Contact	ANNETTE HELLIE Other 510(k) Applications for this Contact
Regulation Number	862.1160   More FDA Info for this Regulation Number
Classification Product Code	JFL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/07/2001
Decision Date	12/18/2001
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
Expedited Review