510(k) K230609 ยท QJP Catheter, Percutaneous, Neurovasculature
NG Delivery Catheter
| Applicant | Balt USA, LLC, Irvine CA, US |
| Decision | Substantially Equivalent, Sep 13, 2023 |
| Received | Mar 6, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230609
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.