Cleared Traditional

ELECTRONIC CELL ENERGIZER (K834293) - FDA 510(k) Clearance

Class II Physical Medicine device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K834293 · Electronic Energy, Inc. · Physical Medicine device
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Jan 1984
Decision
36d
Days
Class 2
Risk

K834293 is an FDA 510(k) clearance for the ELECTRONIC CELL ENERGIZER. Classified as Device, Fluidized Therapy, Dry Heat (product code LBG), Class II - Special Controls.

Submitted by Electronic Energy, Inc. (Mchenry, US). The FDA issued a Cleared decision on January 13, 1984 after a review of 36 days - a notably fast clearance cycle.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.5500 - the FDA physical medicine device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Electronic Energy, Inc. devices

Submission Details

510(k) Number K834293 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 08, 1983
Decision Date January 13, 1984
Days to Decision 36 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
79d faster than avg
Panel avg: 115d · This submission: 36d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code LBG Device, Fluidized Therapy, Dry Heat
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 890.5500
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Physical Medicine devices follow this clearance model.