K212954 is an FDA 510(k) clearance for the G-Tech Wireless Patch System (WPS). This device is classified as a System, Electrogastrography (egg) (Class II - Special Controls, product code MYE).
Submitted by G-Tech Medical (Mountain View, US). The FDA issued a Cleared decision on January 10, 2022, 116 days after receiving the submission on September 16, 2021.
This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.1735.
| 510(k) Number | K212954 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 16, 2021 |
| Decision Date | January 10, 2022 |
| Days to Decision | 116 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | MYE — System, Electrogastrography (egg) |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 876.1735 |