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LigaSure Advance Monopolar Tip Laparoscopic Sealer/Divider, Pistol Grip

K150835 Class II Traditional
Decision Date
2015-10-15
Sponsor / Applicant
Covidien

Technical Specification

510(k) Submission ID K150835
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 2015-10-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LigaSure Advance Monopolar Tip Laparoscopic Sealer/Divider, Pistol Grip received FDA 510(k) clearance under submission number K150835, sponsored by Covidien. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2015-10-15.

Classification & Regulation

This clearance is catalogued under FDA product code GEI and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.