K203630 is an FDA 510(k) clearance for the BioGuard Air/Water and Suction Valves. This device is classified as a Endoscope Channel Accessory (Class II - Special Controls, product code ODC).
Submitted by Steris Corporations (Mentor, US). The FDA issued a Cleared decision on January 8, 2021, 28 days after receiving the submission on December 11, 2020.
This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.1500. To Give The Endoscope Channel Additional Or Improved Functionality..
| 510(k) Number | K203630 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 11, 2020 |
| Decision Date | January 08, 2021 |
| Days to Decision | 28 days |
| Submission Type | Special |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | ODC — Endoscope Channel Accessory |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 876.1500 |
| Definition | To Give The Endoscope Channel Additional Or Improved Functionality. |