K120123 is an FDA 510(k) clearance for the AQUASHIELD CO2 SYSTEM. This device is classified as a Pump, Air, Non-manual, For Endoscope (Class II - Special Controls, product code FEQ).
Submitted by United States Endoscopy Group, Inc. (Mentor, US). The FDA issued a Cleared decision on March 28, 2012, 71 days after receiving the submission on January 17, 2012.
This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.1500.
| 510(k) Number | K120123 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 17, 2012 |
| Decision Date | March 28, 2012 |
| Days to Decision | 71 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Statement |
| Product Code | FEQ - Pump, Air, Non-manual, For Endoscope |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 876.1500 |