510(k) K211811 ยท GDW Staple, Implantable
Disposable Endoscopic Staplers and Reload Unit, Disposable Hemorrhoidal Cutter Staplers, Disposable Linear Cutter Staplers, Disposable Circular Staplers
| Applicant | Wuxi Beien Surgery Device Co., Ltd., Wuxi, CN |
| Decision | Substantially Equivalent, Mar 3, 2022 |
| Received | Jun 11, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211811
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.