K112318 is an FDA 510(k) clearance for the CLEARPATH 24, a Endoscopic Irrigation/suction System (Class II — Special Controls, product code OCX), submitted by Promedic, Inc. (Bonita Springs, US). The FDA issued a Cleared decision on June 29, 2012, 323 days after receiving the submission on August 11, 2011. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.1500.
| 510(k) Number | K112318 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | August 11, 2011 |
| Decision Date | June 29, 2012 |
| Days to Decision | 323 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | OCX — Endoscopic Irrigation/suction System |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 876.1500 |
| Definition | To Supply Sterile Water, Other Solutions And/or Suction To Endoscopes During Endoscopic Procedures. |