meddevicedb.com FDA Device Reference

R2 Dermal Cooling System

K161480 Class II Traditional
Decision Date
2016-10-05
Sponsor / Applicant
R2 Dermatology

Technical Specification

510(k) Submission ID K161480
Product Code GEH
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4350
Decision Date 2016-10-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

R2 Dermal Cooling System received FDA 510(k) clearance under submission number K161480, sponsored by R2 Dermatology. 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 2016-10-05.

Classification & Regulation

This clearance is catalogued under FDA product code GEH and 21 CFR 878.4350, within the General, Plastic Surgery review panel as a Class II device.