meddevicedb.com FDA Device Reference

LIFESTYLE HOME TANNING UNITS

K901714 Class II Traditional
Decision Date
1990-06-27
Sponsor / Applicant
Life Products, Inc.

Technical Specification

510(k) Submission ID K901714
Product Code LEJ
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4635
Decision Date 1990-06-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LIFESTYLE HOME TANNING UNITS received FDA 510(k) clearance under submission number K901714, sponsored by Life Products, Inc.. 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 1990-06-27.

Classification & Regulation

This clearance is catalogued under FDA product code LEJ and 21 CFR 878.4635, within the General, Plastic Surgery review panel as a Class II device.