meddevicedb.com FDA Device Reference

ELECTRICAL MUSCLE STIMULATOR

K820884 Class II Traditional
Decision Date
1982-04-29
Sponsor / Applicant
Nitron Electronics

Technical Specification

510(k) Submission ID K820884
Product Code IPF
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5850
Decision Date 1982-04-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELECTRICAL MUSCLE STIMULATOR received FDA 510(k) clearance under submission number K820884, sponsored by Nitron Electronics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 1982-04-29.

Classification & Regulation

This clearance is catalogued under FDA product code IPF and 21 CFR 890.5850, within the Physical Medicine review panel as a Class II device.