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Scanditronix Medical AB

4 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
OMNIDOS (K011763)Scanditronix Medical AB2001-09-05
INVIDOS (K002051)Scanditronix Medical AB2000-09-05
DPD-12PCC (K990734)Scanditronix Medical AB1999-05-28
RFA-300, LDA UTILITY (K961400)Scanditronix Medical AB1997-01-03

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