K-number	K094039
Device name	HYALO GYN
Applicant	Fidia Farmaceutici S.P.A.
Product code	NUC
Device class	Class II
Decision date	May 7, 2010
Decision	Substantially Equivalent
Regulation	884.5300

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View the full FDA submission: accessdata.fda.gov

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HYALO GYN

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