K-number	K103253
Device name	SILS PORT
Applicant	Coviden (Formerly Registered AS US Surgical, A Div
Product code	GCJ
Device class	Class II
Decision date	Feb 24, 2011
Decision	Substantially Equivalent
Regulation	876.1500

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Source

View the full FDA submission: accessdata.fda.gov

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SILS PORT

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