Cleared Traditional

MLS-AC DERMA SCANNER

K101430 · Erchonia Corporation · Physical Medicine

Jun 2010

Decision

32d

Days

Class 2

Risk

About This 510(k) Submission

K101430 is an FDA 510(k) clearance for the MLS-AC DERMA SCANNER, a Powered Light Based Laser Non-thermal Instrument With Non-heating Effect For Adjunctive Use In Pain Therapy (Class II — Special Controls, product code NHN), submitted by Erchonia Corporation (Littleton, US). The FDA issued a Cleared decision on June 22, 2010, 32 days after receiving the submission on May 21, 2010. This device falls under the Physical Medicine review panel. Regulated under 21 CFR 890.5500.

Submission Details

510(k) Number	K101430 FDA.gov
FDA Decision	Cleared SESE
Date Received	May 21, 2010
Decision Date	June 22, 2010
Days to Decision	32 days
Submission Type	Traditional
Review Panel	Physical Medicine (PM)
Summary	Statement

Device Classification

Product Code	NHN — Powered Light Based Laser Non-thermal Instrument With Non-heating Effect For Adjunctive Use In Pain Therapy
Device Class	Class II — Special Controls
CFR Regulation	21 CFR 890.5500
Definition	A Laser (light Amplification By Stimulated Emission Of Radiation) Based Device Having Coherence, Collimated And Typically Monochromatic Radiation. This Device Emits Energy In The Infrared Or Other Wavelengths, Provides Non-heating And Non-thermal Effect, And Is Indicated For Adjunctive Use In Pain Therapy Or Related Indication. It Does Not Provide Therapeutic Topical Heating. The Classification Regulation For Infrared Lamps Describes A Device That Emits Energy In The Infrared Wavelength To Provide Topical Heating And That Is Not Limited To Adjunctive Use.