FDA 510(k) Applications Submitted by SCANDITRONIX MEDICAL AB

FDA 510(k) Number Submission Date Device Name Applicant
K011763 06/07/2001 OMNIDOS SCANDITRONIX MEDICAL AB
K990734 03/05/1999 DPD-12PCC SCANDITRONIX MEDICAL AB
K002051 07/06/2000 INVIDOS SCANDITRONIX MEDICAL AB
K961400 04/11/1996 RFA-300, LDA UTILITY SCANDITRONIX MEDICAL AB


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