K-number	K932021
Device name	ENTREE CANNULA FASCIA ANCHORS
Applicant	Core Dynamics, Inc.
Product code	FBM
Device class	Class I
Decision date	Jan 11, 1994
Decision	Substantially Equivalent
Regulation	876.5090

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View the full FDA submission: accessdata.fda.gov

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ENTREE CANNULA FASCIA ANCHORS

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