K-number	K060380
Device name	FIDIS DSDNA
Applicant	Biomedical Diagnostics (Bmd) SA
Product code	LSW
Device class	Class II
Decision date	May 2, 2006
Decision	Substantially Equivalent
Regulation	866.5100

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Source

View the full FDA submission: accessdata.fda.gov

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FIDIS DSDNA

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