K-number	K131963
Device name	TAUTONA INJECTOR DEVICE
Applicant	Tautona Group, LLC
Product code	FMF
Device class	Class II
Decision date	Oct 22, 2013
Decision	Substantially Equivalent
Regulation	880.5860

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Source

View the full FDA submission: accessdata.fda.gov

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TAUTONA INJECTOR DEVICE

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