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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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