meddevicedb.com FDA Device Reference

UV PHOTOTHERAPY

K132643 Class II Traditional
Decision Date
2014-01-30
Sponsor / Applicant
Xuzhou Kernel Medical Equipment Co., Ltd.

Technical Specification

510(k) Submission ID K132643
Product Code FTC
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4630
Decision Date 2014-01-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UV PHOTOTHERAPY received FDA 510(k) clearance under submission number K132643, sponsored by Xuzhou Kernel Medical Equipment Co., 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 2014-01-30.

Classification & Regulation

This clearance is catalogued under FDA product code FTC and 21 CFR 878.4630, within the General, Plastic Surgery review panel as a Class II device.