Cleared Traditional

K091865 - SPORT-ELEC BODY CONTROL SYSTEM

K091865 is an FDA 510(k) clearance for SPORT-ELEC BODY CONTROL SYSTEM, manufactured by Sport-Elec. The device is a Class 2 Physical Medicine device with product code NGX cleared through the Traditional 510(k) pathway after a 147-day FDA review.

K091865 · Sport-Elec · Physical Medicine device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Nov 2009
Decision
147d
Days
Class 2
Risk

K091865 is an FDA 510(k) clearance for the SPORT-ELEC BODY CONTROL SYSTEM. Classified as Stimulator, Muscle, Powered, For Muscle Conditioning (product code NGX), Class II - Special Controls.

Submitted by Sport-Elec (Hampton, US). The FDA issued a Cleared decision on November 13, 2009 after a review of 147 days - within the typical 510(k) review window.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.5850 - the FDA physical medicine 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Physical Medicine review framework, consistent with the majority of Class II 510(k) submissions.

FDA 510(k) Submission Details - K091865

510(k) Number K091865 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 19, 2009
Decision Date November 13, 2009
Days to Decision 147 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
31d slower than avg
Panel avg: 116d · This submission: 147d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

NGX Device Classification - Class 2, Special Controls

Product Code NGX Stimulator, Muscle, Powered, For Muscle Conditioning
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 890.5850
Definition A Powered Muscle Stimulator For Muscle Conditioning Is A Device Used For Other Than Medical Purposes To Apply An Electrical Current To Electrodes On A Person's Skin To Temporarily Affect The Stimulated Muscle's Contractile Properties, Force Output, And/or Fatigue Resistance. Unlike The Classified Powered Muscle Stimulator Devices Intended For Use In Physical Medicine And Rehabilitation, This Device Is Not Intended For Use In Patients With Medical Conditions And Is Intended Only For Muscle Conditioning Purposes.
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 Physical Medicine devices follow this clearance model.

Regulatory Peers - NGX Stimulator, Muscle, Powered, For Muscle Conditioning

All 162
Devices cleared under the same product code (NGX) and FDA review panel - the closest regulatory comparables to K091865.
SLENDERTONE SYSTEM ULTRA MODEL E70/X70
K100320 · Bio-Medical Research, Ltd. · May 2010
SPORT-ELEC BODY CONTROL SYSTEM BS
K092142 · Sport-Elec · Feb 2010
BUTTERFLY TONER MODEL GYM070
K093368 · Global Marketing Partners Dba Gymmax USA · Jan 2010
GEM-STONE ABDOMINAL TRAINING SYSTEM
K091833 · Gemore Technology Co, Ltd. · Oct 2009
H-WAVE SPORT
K081998 · Electronic Waveform Laboratory, Inc. · Jul 2009
COMPEX SPORT PLUS
K083140 · Chattanooga Group · Feb 2009
K091865 · SPORT-ELEC BODY CONTROL SYSTEM
Download PDF FDA Summary Sport-Elec