K-number	K123141
Device name	ENSEAL TRIO TISSUE SEALING DEVICE
Applicant	Ethicon Endo-Surgery, LLC
Product code	GEI
Device class	Class II
Decision date	Oct 25, 2012
Decision	Substantially Equivalent
Regulation	878.4400

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Source

View the full FDA submission: accessdata.fda.gov

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ENSEAL TRIO TISSUE SEALING DEVICE

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