510(k) K240185 ยท GEJ Carrier, Ligature
Cypris eXact Suture Placement Device
| Applicant | Cypris Medical, Chicago IL, US |
| Decision | Substantially Equivalent, May 3, 2024 |
| Received | Jan 23, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240185
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.