meddevicedb.com FDA Device Reference

New Era

K182604 Class II Traditional
Decision Date
2018-11-14
Sponsor / Applicant
Step UP Skin Laser, LLC

Technical Specification

510(k) Submission ID K182604
Product Code GEX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 2018-11-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

New Era received FDA 510(k) clearance under submission number K182604, sponsored by Step UP Skin Laser, LLC. 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 2018-11-14.

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.