510(k) K261890 · KNT Tubes, Gastrointestinal (And Accessories)
52Fr ViSiGi LUX; 52Fr ViSiGi 3D®
| Applicant | Boehringer Laboratories, LLC, Phoenixville PA, US |
| Decision | Substantially Equivalent, Aug 14, 2026 |
| Received | Jun 5, 2026 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K261890
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.