K-number	K160171
Device name	Illuminated Mediastinal Access Port
Applicant	Aegis Surgical, Ltd.
Product code	EWY
Device class	Class II
Decision date	Feb 26, 2016
Decision	Substantially Equivalent
Regulation	874.4720

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View the full FDA submission: accessdata.fda.gov

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Illuminated Mediastinal Access Port

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