Cleared Traditional

MEDI MODEL SBL502-B (LISS BODY STIMULATOR) ZERO DC (K902976) - FDA 510(k) Clearance

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

K902976 · Medical Consultants Intl. , Ltd. · Neurology device
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Sep 1990
Decision
63d
Days
Class 2
Risk

K902976 is an FDA 510(k) clearance for the MEDI MODEL SBL502-B (LISS BODY STIMULATOR) ZERO DC. Classified as Electrode, Depth (product code GZL), Class II - Special Controls.

Submitted by Medical Consultants Intl. , Ltd. (Glen Rock, US). The FDA issued a Cleared decision on September 7, 1990 after a review of 63 days - a notably fast clearance cycle.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 882.1330 - 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 Medical Consultants Intl. , Ltd. devices

Submission Details

510(k) Number K902976 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 06, 1990
Decision Date September 07, 1990
Days to Decision 63 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
85d faster than avg
Panel avg: 148d · This submission: 63d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code GZL Electrode, Depth
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 882.1330
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 - GZL Electrode, Depth

All 57
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