meddevicedb.com FDA Device Reference

ELECTROPULSE-COSMETIC

K113724 Class II Traditional
Decision Date
2012-02-15
Sponsor / Applicant
Pain Relief Technologies

Technical Specification

510(k) Submission ID K113724
Product Code NFO
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5890
Decision Date 2012-02-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELECTROPULSE-COSMETIC received FDA 510(k) clearance under submission number K113724, sponsored by Pain Relief Technologies. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2012-02-15.

Classification & Regulation

This clearance is catalogued under FDA product code NFO and 21 CFR 882.5890, within the Neurology review panel as a Class II device.