K-number	K062125
Device name	SUPERSTITCH 5F, 12F, AND EL
Applicant	Sutura, Inc.
Product code	GAW
Device class	Class II
Decision date	Oct 19, 2006
Decision	Substantially Equivalent
Regulation	878.5010

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Source

View the full FDA submission: accessdata.fda.gov

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SUPERSTITCH 5F, 12F, AND EL

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