Cleared Traditional

K854208 - THE BODYLOG 500 RET THERAPEUTIC ELECTROMYOGRAPHICS

K854208 is an FDA 510(k) clearance for THE BODYLOG 500 RET THERAPEUTIC ELECTRO..., manufactured by Bodylog, Inc.. The device is a Class 2 Neurology device with product code HCC cleared through the Traditional 510(k) pathway after a 89-day FDA review.

K854208 · Bodylog, Inc. · Neurology device
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Jan 1986
Decision
89d
Days
Class 2
Risk

K854208 is an FDA 510(k) clearance for the THE BODYLOG 500 RET THERAPEUTIC ELECTROMYOGRAPHICS. Classified as Device, Biofeedback (product code HCC), Class II - Special Controls.

Submitted by Bodylog, Inc. (Mt. Kisco, US). The FDA issued a Cleared decision on January 14, 1986 after a review of 89 days - a notably fast clearance cycle.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 882.5050 - the FDA neurology 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 Bodylog, Inc. devices

FDA 510(k) Submission Details - K854208

510(k) Number K854208 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 17, 1985
Decision Date January 14, 1986
Days to Decision 89 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
59d faster than avg
Panel avg: 148d · This submission: 89d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HCC Device Classification - Class 2, Special Controls

Product Code HCC Device, Biofeedback
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 882.5050
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 Neurology devices follow this clearance model.

Regulatory Peers - HCC Device, Biofeedback

All 57
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