meddevicedb.com FDA Device Reference

Lapro-Clip Auto Suture Reusable Long Clip Applier

K143598 Class II Special
Decision Date
2015-03-12
Sponsor / Applicant
Covidien, LLC

Technical Specification

510(k) Submission ID K143598
Product Code FZP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4300
Decision Date 2015-03-12
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Lapro-Clip Auto Suture Reusable Long Clip Applier received FDA 510(k) clearance under submission number K143598, sponsored by Covidien, LLC. 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 2015-03-12.

Classification & Regulation

This clearance is catalogued under FDA product code FZP and 21 CFR 878.4300, within the General, Plastic Surgery review panel as a Class II device.