K243591 is an FDA 510(k) clearance for the OPTOVISION Endoscopic Light Source Unit, a Confocal Optical Imaging (Class II — Special Controls, product code OWN), submitted by Optosurgical, LLC (Columbia, US). The FDA issued a Cleared decision on February 19, 2025, 91 days after receiving the submission on November 20, 2024. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 876.1500.
| 510(k) Number | K243591 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | November 20, 2024 |
| Decision Date | February 19, 2025 |
| Days to Decision | 91 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | OWN — Confocal Optical Imaging |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 876.1500 |
| Definition | Collection Of Light Signals For Visualization Of Cellular Microstructures. |