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


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact