510(k) K171620 ยท KRB Probe, Thermodilution
PiCCO Catheter
| Applicant | Pulsion Medical Systems SE, Feldkirchen, DE |
| Decision | Substantially Equivalent, Feb 21, 2018 |
| Received | Jun 2, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171620
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.