meddevicedb.com FDA Device Reference

HAWKINS EBA -16 MUSCLE STIMULATOR

K822519 Class II Traditional
Decision Date
1982-10-13
Sponsor / Applicant
A-Zenith Therapeutic Equipment/Supply

Technical Specification

510(k) Submission ID K822519
Product Code IPF
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5850
Decision Date 1982-10-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HAWKINS EBA -16 MUSCLE STIMULATOR received FDA 510(k) clearance under submission number K822519, sponsored by A-Zenith Therapeutic Equipment/Supply. 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 1982-10-13.

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.