K-number	K143260
Device name	Reprocessed Covidien LigaSure 5mm, Blunt Tip, Laparoscopic Sealer/Divider
Applicant	Sterilmed, Inc.
Product code	NUJ
Device class	Class II
Decision date	Feb 23, 2015
Decision	Substantially Equivalent
Regulation	878.4400

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Source

View the full FDA submission: accessdata.fda.gov

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Reprocessed Covidien LigaSure 5mm, Blunt Tip, Laparoscopic Sealer/Divider

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