K221987 is an FDA 510(k) clearance for the Erchonia GVL, 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 (Melbourne, US). The FDA issued a Cleared decision on September 1, 2022, 57 days after receiving the submission on July 6, 2022. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 890.5500.
| 510(k) Number | K221987 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | July 06, 2022 |
| Decision Date | September 01, 2022 |
| Days to Decision | 57 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| 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. |