K183595 is an FDA 510(k) clearance for the Aqua Medical RF Vapor System, a Unit, Electrosurgical, Endoscopic (with Or Without Accessories) (Class II — Special Controls, product code KNS), submitted by Aqua Medical, Inc. (Santa Ana, US). The FDA issued a Cleared decision on June 21, 2019, 182 days after receiving the submission on December 21, 2018. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.4300.
| 510(k) Number | K183595 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | December 21, 2018 |
| Decision Date | June 21, 2019 |
| Days to Decision | 182 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | KNS — Unit, Electrosurgical, Endoscopic (with Or Without Accessories) |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 876.4300 |