K-number	K110606
Device name	MV INTRADERMIC NEEDLES; MAGIC NEEDLE; MAGIC NEEDLE
Applicant	M.V.S.R.L.
Product code	FMI
Device class	Class II
Decision date	Sep 29, 2011
Decision	Substantially Equivalent
Regulation	880.5570

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View the full FDA submission: accessdata.fda.gov

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MV INTRADERMIC NEEDLES; MAGIC NEEDLE; MAGIC NEEDLE

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