510(k) K223275 ยท QJP Catheter, Percutaneous, Neurovasculature
CELLO II Balloon Guide Catheter
| Applicant | Fuji Systems Corporation, Nishi Shirakawa Gun, JP |
| Decision | Substantially Equivalent, Dec 9, 2022 |
| Received | Oct 24, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223275
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.