510(k) K261549 ยท QJP Catheter, Percutaneous, Neurovasculature
BOBBY Balloon Guide Catheter
| Applicant | MicroVention, Inc., d/b/a Terumo Neuro, Aliso Viejo CA, US |
| Decision | Substantially Equivalent, Jun 9, 2026 |
| Received | May 11, 2026 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K261549
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.