Class Class II

LigaSure™ XP Maryland Jaw Sealer/Divider (K223158)

K223158 2023-01-23 Traditional
Home/ Devices/ LigaSure™ XP Maryland Jaw…

Description

LigaSure™ XP Maryland Jaw Sealer/Divider by Covidien, LLC — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223158
Clearance Date2023-01-23
Clearance TypeTraditional
Product CodeGEI
Regulation Number878.4400

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top