meddevicedb.com FDA Device Reference

UVA SUN SYSTEMS

K860859 Class II Traditional
Decision Date
1986-03-28
Sponsor / Applicant
Bremi

Technical Specification

510(k) Submission ID K860859
Product Code FTC
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4630
Decision Date 1986-03-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UVA SUN SYSTEMS received FDA 510(k) clearance under submission number K860859, sponsored by Bremi. 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 1986-03-28.

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.