meddevicedb.com FDA Device Reference

BERKOWITS 2200 SHORT WAVE (THERMOLYSIS EPILATOR)

K860056 Class I Traditional
Decision Date
1986-02-05
Sponsor / Applicant
Berkowits School of Electrolysis, Inc.

Technical Specification

510(k) Submission ID K860056
Product Code KCW
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5350
Decision Date 1986-02-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BERKOWITS 2200 SHORT WAVE (THERMOLYSIS EPILATOR) received FDA 510(k) clearance under submission number K860056, sponsored by Berkowits School of Electrolysis, 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 1986-02-05.

Classification & Regulation

This clearance is catalogued under FDA product code KCW and 21 CFR 878.5350, within the General, Plastic Surgery review panel as a Class I device.