FDA 510(k) Application Details - K033840

Device Classification Name	Device, Automated Cell-Locating   More FDA Info for this Device
510(K) Number	K033840
Device Name	Device, Automated Cell-Locating
Applicant	CELLAVISION AB 6740 RIVERVIEW TERRACE MINNEAPOLIS, MN 55432 US Other 510(k) Applications for this Company
Contact	CONSTANCE G BUNDY Other 510(k) Applications for this Contact
Regulation Number	864.5260   More FDA Info for this Regulation Number
Classification Product Code	JOY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/10/2003
Decision Date	02/10/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HE - Hematology
Review Advisory Committee	HE - Hematology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review