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FDA 510(k) Applications Submitted by CELLAVISION AB
FDA 510(k) Number
Submission Date
Device Name
Applicant
K080595
03/03/2008
CELLAVISION DM96 WITH THE BODY FLUID APPLICATION
CELLAVISION AB
K092868
09/18/2009
CELLAVISION DM1200 AUTOMATED HEMATOLOGY ANALYZER, MODEL XU-10127
CELLAVISION AB
K102778
09/24/2010
CELLAVISION DM1200 WITH THE BODY FLUID APPLICTION
CELLAVISION AB
K003301
10/20/2000
DIFFMASTER OCTAVIA AUTOMATIC HEMATOLOGY ANALYZER
CELLAVISION AB
K033840
12/10/2003
CELLAVISION DM96 AUTOMATIC HEMATOLOGY ANALYZER
CELLAVISION AB
K200595
03/06/2020
CellaVision DC-1, CellaVision DC-1 PPA
CellaVision AB
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