510(k) K161731 ยท HCA Catheter, Ventricular
Cleveland Multiport Ventricular Catheter Set
| Applicant | Parker Hannifin Corp., Ventura CA, US |
| Decision | Substantially Equivalent, Mar 27, 2017 |
| Received | Jun 23, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161731
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.