meddevicedb.com FDA Device Reference

Ligasure Blunt Tip, Sealer/Divider, Nano-coated

K162941 Class II Special
Decision Date
2016-11-14
Sponsor / Applicant
Covidien

Technical Specification

510(k) Submission ID K162941
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 2016-11-14
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Ligasure Blunt Tip, Sealer/Divider, Nano-coated received FDA 510(k) clearance under submission number K162941, sponsored by Covidien. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2016-11-14.

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.