meddevicedb.com FDA Device Reference

Coolrail Linear Pen

K183065 Class II Special
Decision Date
2018-12-04
Sponsor / Applicant
AtriCure, Inc.

Technical Specification

510(k) Submission ID K183065
Product Code OCL
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 2018-12-04
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Coolrail Linear Pen received FDA 510(k) clearance under submission number K183065, sponsored by AtriCure, Inc.. 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 2018-12-04.

Classification & Regulation

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