K-number	K050150
Device name	MANI NEEDLE & SUTURE PACK
Applicant	Mani, Inc.
Product code	GAT
Device class	Class II
Decision date	Dec 5, 2005
Decision	Substantially Equivalent
Regulation	878.5000

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View the full FDA submission: accessdata.fda.gov

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MANI NEEDLE & SUTURE PACK

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