510(k) K234131 ยท QAU Hemostatic Device For Endoscopic Gastrointestinal Use
Resolv Endoscopic Hemostat System
| Applicant | Hemostasis, LLC, St. Paul MN, US |
| Decision | Substantially Equivalent, Jul 26, 2024 |
| Received | Dec 28, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K234131
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.