meddevicedb.com FDA Device Reference

NO!NO! SKIN

K102477 Class II Traditional
Decision Date
2010-10-04
Sponsor / Applicant
Radiancy (Israel) , Ltd.

Technical Specification

510(k) Submission ID K102477
Product Code OLP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 2010-10-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NO!NO! SKIN received FDA 510(k) clearance under submission number K102477, sponsored by Radiancy (Israel) , Ltd.. 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 2010-10-04.

Classification & Regulation

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