Cleared Traditional

K770663 - FEEDBACK EMG SYSTEM

K770663 is the FDA 510(k) clearance for FEEDBACK EMG SYSTEM by Bio-Feedback Systems, Inc.. It is a Class 2 Neurology device (product code HCC) cleared through the Traditional 510(k) pathway after a 19-day FDA review.

K770663 · Bio-Feedback Systems, Inc. · Neurology device
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Apr 1977
Decision
19d
Days
Class 2
Risk

K770663 is an FDA 510(k) clearance for the FEEDBACK EMG SYSTEM, MODEL PE-L00. Classified as Device, Biofeedback (product code HCC), Class II - Special Controls.

Submitted by Bio-Feedback Systems, Inc. (Mchenry, US). The FDA issued a Cleared decision on April 26, 1977 after a review of 19 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 Bio-Feedback Systems, Inc. devices

Submission Details

510(k) Number K770663 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 07, 1977
Decision Date April 26, 1977
Days to Decision 19 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
129d faster than avg
Panel avg: 148d · This submission: 19d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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.