Cleared Traditional

K990370 - MSB (ELECTRICAL STIMULATION) ELECTRODES (DISPOSABLE). (TENS/FES/NMES)

K990370 is an FDA 510(k) clearance for MSB (ELECTRICAL STIMULATION) ELECTRODES..., manufactured by Msb,Uk. The device is a Class 2 Neurology device with product code GXY cleared through the Traditional 510(k) pathway after a 63-day FDA review.

K990370 · Msb,Uk · Neurology device
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Apr 1999
Decision
63d
Days
Class 2
Risk

K990370 is an FDA 510(k) clearance for the MSB (ELECTRICAL STIMULATION) ELECTRODES (DISPOSABLE). (TENS/FES/NMES). Classified as Electrode, Cutaneous (product code GXY), Class II - Special Controls.

Submitted by Msb,Uk (Marlborough,Wiltshire, GB). The FDA issued a Cleared decision on April 12, 1999 after a review of 63 days - a notably fast clearance cycle.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 882.1320 - 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 Msb,Uk devices

FDA 510(k) Submission Details - K990370

510(k) Number K990370 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 08, 1999
Decision Date April 12, 1999
Days to Decision 63 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
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.

GXY Device Classification - Class 2, Special Controls

Product Code GXY Electrode, Cutaneous
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 882.1320
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 - GXY Electrode, Cutaneous

All 267
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