510(k) K211326 ยท QNP Gastrointesinal Lesion Software Detection System
EndoScreener
| Applicant | Chengdu Wision Medical Device Co., Ltd., Chengdu, CN |
| Decision | Substantially Equivalent, Nov 19, 2021 |
| Received | Apr 30, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211326
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.