K192350 is an FDA 510(k) clearance for the Medical Non-Ablative Fractional Laser Systems, a Powered Laser Surgical Instrument With Microbeamfractional Output (Class II — Special Controls, product code ONG), submitted by Wingderm Electro-Optics , Ltd. (Beijing, CN). The FDA issued a Cleared decision on April 30, 2020, 245 days after receiving the submission on August 29, 2019. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4810.
| 510(k) Number | K192350 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | August 29, 2019 |
| Decision Date | April 30, 2020 |
| Days to Decision | 245 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | ONG — Powered Laser Surgical Instrument With Microbeamfractional Output |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 878.4810 |
| Definition | A Laser (light Amplification By Stimulated Emission Of Radiation) Based Device Having Coherence, Collimated And Typically Monochromatic Radiation. The Laser Output Is In Form Of Tiny Beams In Micro Range. Typically, Indicated To Be Used In Medical Specialties Of General And Plastic Surgery And Of Dermatology/aesthetic To Destroy, Remove Or Coagulate Tissue, Generally Soft Tissue. Indication For Use Can Be General And/or Specific. The Classification Regulation 21 Cfr 878.4810 Describes A Device That Is Carbon Dioxide Or Argon Laser Intended To Cut, Destroy, Remove Or Coagulate Tissue By The Light. |