K-number	K053383
Device name	FIDIS CELIAC
Applicant	Biomedical Diagnostics (Bmd) SA
Product code	MST
Device class	Class II
Decision date	Mar 29, 2006
Decision	Substantially Equivalent
Regulation	866.5750

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Source

View the full FDA submission: accessdata.fda.gov

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FIDIS CELIAC

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