K-number	K223158
Device name	LigaSure XP Maryland Jaw Sealer/Divider
Applicant	Covidien, LLC
Product code	GEI
Device class	Class II
Decision date	Jan 23, 2023
Decision	Substantially Equivalent
Regulation	878.4400

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Source

View the full FDA submission: accessdata.fda.gov

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LigaSure XP Maryland Jaw Sealer/Divider

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LigaSure XP Maryland Jaw Sealer/Divider