meddevicedb.com FDA Device Reference

ELECTROLYSIS MACHINE (PERMATRON)

K760423 Class I Traditional
Decision Date
1976-09-15
Sponsor / Applicant
Epco Hair Removal Corp.

Technical Specification

510(k) Submission ID K760423
Product Code KCX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5360
Decision Date 1976-09-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELECTROLYSIS MACHINE (PERMATRON) received FDA 510(k) clearance under submission number K760423, sponsored by Epco Hair Removal Corp.. 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 1976-09-15.

Classification & Regulation

This clearance is catalogued under FDA product code KCX and 21 CFR 878.5360, within the General, Plastic Surgery review panel as a Class I device.