510(k) K191237 ยท DQY Catheter, Percutaneous
CERENOVUS Large Bore Catheter
| Applicant | Codman & Shurtleff, Inc., Raynham MA, US |
| Decision | Substantially Equivalent, Nov 8, 2019 |
| Received | May 8, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191237
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.