meddevicedb.com FDA Device Reference

FRACTIONAL SKIN RESURFACING (FSR) APPLICATOR

K101510 Class II Traditional
Decision Date
2011-02-17
Sponsor / Applicant
Endymed Medical, Ltd.

Technical Specification

510(k) Submission ID K101510
Product Code OUH
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 2011-02-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FRACTIONAL SKIN RESURFACING (FSR) APPLICATOR received FDA 510(k) clearance under submission number K101510, sponsored by Endymed Medical, 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 2011-02-17.

Classification & Regulation

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