Cleared Traditional

K884348 - MODIFIED JELTRODE(TM) ELECTRODES DEEMED

K884348 is the FDA 510(k) clearance for MODIFIED JELTRODE(TM) ELECTRODES DEEMED by Henley Intl.. It is a Class 2 Neurology device (product code GXY) cleared through the Traditional 510(k) pathway after a 62-day FDA review.

K884348 · Henley Intl. · Neurology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Dec 1988
Decision
62d
Days
Class 2
Risk

K884348 is an FDA 510(k) clearance for the MODIFIED JELTRODE(TM) ELECTRODES DEEMED. Classified as Electrode, Cutaneous (product code GXY), Class II - Special Controls.

Submitted by Henley Intl. (Sugar Land, US). The FDA issued a Cleared decision on December 15, 1988 after a review of 62 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 Henley Intl. devices

Submission Details

510(k) Number K884348 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 14, 1988
Decision Date December 15, 1988
Days to Decision 62 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
86d faster than avg
Panel avg: 148d · This submission: 62d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 143
Devices cleared under the same product code (GXY) and FDA review panel - the closest regulatory comparables to K884348.
EMPI ISLAND TENS ELECTRODE
K890605 · Empi · Mar 1989
EMPI MULTIDAY TENS DISPOSABLE ELECTRODE
K890614 · Empi · Mar 1989
EMPI REUSEABLE PIN-STYLE TENS ELECTRODE
K890747 · Empi · Mar 1989
MULTIDAY, MODELS 8300 AND 8310
K882888 · Medical Devices, Inc. · Sep 1988
PROGEL (TM) DUAL ELECTRODE PAD, MODEL 8535
K882886 · Medical Devices, Inc. · Sep 1988
PROGEL(TM), MODELS 8630 AND 8635
K882887 · Medical Devices, Inc. · Sep 1988