K101006 is an FDA 510(k) clearance for the WAVELIGHT FS200 LASER SYSTEM MODEL: FS200, a Powered Laser Surgical Instrument (Class II — Special Controls, product code GEX), submitted by Alcon Research, Ltd. (Fort Worth, US). The FDA issued a Cleared decision on October 21, 2010, 192 days after receiving the submission on April 12, 2010. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4810.
| 510(k) Number | K101006 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | April 12, 2010 |
| Decision Date | October 21, 2010 |
| Days to Decision | 192 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | GEX — Powered Laser Surgical Instrument |
| 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. Typically Indicated To To Cut, Destroy, Remove Or Coagulate Tissue, Generally Soft Tissue, For General Surgical Purpose In Medical Specialties Of General And Plastic Surgery, Dermatology/aesthetic, Podiatry, Otolaryngology (ent), Gynecology, Neurosurgery, Orthopedics (soft Tissue), Dental And Oral Surgery, And Dentistry. 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. |