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THE VARIABLE LOAD KENETIC ENERGIZER

K792642 Class I Traditional
Decision Date
1980-01-28
Sponsor / Applicant
W.F. Pogue

Technical Specification

510(k) Submission ID K792642
Product Code ION
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5370
Decision Date 1980-01-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

THE VARIABLE LOAD KENETIC ENERGIZER received FDA 510(k) clearance under submission number K792642, sponsored by W.F. Pogue. 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 1980-01-28.

Classification & Regulation

This clearance is catalogued under FDA product code ION and 21 CFR 890.5370, within the Physical Medicine review panel as a Class I device.