K-number	K160539
Device name	BiZact Open Sealer/Divider
Applicant	Covidien
Product code	GEI
Device class	Class II
Decision date	Jun 15, 2016
Decision	Substantially Equivalent
Regulation	878.4400

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Source

View the full FDA submission: accessdata.fda.gov

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BiZact Open Sealer/Divider

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