510(k) K160681 ยท DQY Catheter, Percutaneous
CenterCross Ultra Catheter
| Applicant | Roxwood Medical, Inc., Redwood City CA, US |
| Decision | Substantially Equivalent, Jun 17, 2016 |
| Received | Mar 10, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K160681
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.