510(k) K170403 ยท DQY Catheter, Percutaneous
CenterCross Ultra LV Catheter
| Applicant | Roxwood Medical, Inc., Redwood City CA, US |
| Decision | Substantially Equivalent, Mar 7, 2017 |
| Received | Feb 9, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K170403
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.