Cleared Traditional

K093368 - BUTTERFLY TONER MODEL GYM070

K093368 is an FDA 510(k) clearance for BUTTERFLY TONER MODEL GYM070, manufactured by Global Marketing Partners Dba Gymmax USA. The device is a Class 2 Physical Medicine device with product code NGX cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K093368 · Global Marketing Partners Dba Gymmax USA · Physical Medicine device
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Jan 2010
Decision
90d
Days
Class 2
Risk

K093368 is an FDA 510(k) clearance for the BUTTERFLY TONER MODEL GYM070. Classified as Stimulator, Muscle, Powered, For Muscle Conditioning (product code NGX), Class II - Special Controls.

Submitted by Global Marketing Partners Dba Gymmax USA (Laguna Niguel, US). The FDA issued a Cleared decision on January 27, 2010 after a review of 90 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.

View all Global Marketing Partners Dba Gymmax USA devices

FDA 510(k) Submission Details - K093368

510(k) Number K093368 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 29, 2009
Decision Date January 27, 2010
Days to Decision 90 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
25d faster than avg
Panel avg: 115d · This submission: 90d
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 110
Devices cleared under the same product code (NGX) and FDA review panel - the closest regulatory comparables to K093368.
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