K163257 is an FDA 510(k) clearance for the VitreOx Anti-fog Solution, a Anti Fog Solution And Accessories, Endoscopy (Class II — Special Controls, product code OCT), submitted by Sio2 Nanotech, LLC (Phoenix, US). The FDA issued a Cleared decision on May 24, 2017, 191 days after receiving the submission on November 14, 2016. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.1500.
| 510(k) Number | K163257 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | November 14, 2016 |
| Decision Date | May 24, 2017 |
| Days to Decision | 191 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | OCT — Anti Fog Solution And Accessories, Endoscopy |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 876.1500 |
| Definition | To Prevent, Reduce Or Eliminate Condensation (fog) On Endoscopic Lens. |