510(k) K234033 ยท KNT Tubes, Gastrointestinal (And Accessories)
ViSiGi LUX (5332); ViSiGi LUX (5336); ViSiGi LUX (5340)
| Applicant | Boehringer Laboratories, LLC, Phoenixville PA, US |
| Decision | Substantially Equivalent, May 6, 2024 |
| Received | Dec 20, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K234033
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.