meddevicedb.com FDA Device Reference

SmoothCool HR System

K223685 Class II Special
Decision Date
2023-01-04
Sponsor / Applicant
Jeisys Medical, Inc.

Technical Specification

510(k) Submission ID K223685
Product Code GEX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 2023-01-04
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SmoothCool HR System received FDA 510(k) clearance under submission number K223685, sponsored by Jeisys Medical, 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 2023-01-04.

Classification & Regulation

This clearance is catalogued under FDA product code GEX and 21 CFR 878.4810, within the General, Plastic Surgery review panel as a Class II device.