510(k) K163316 ยท DSA Cable, Transducer And Electrode, Patient, (Including Connector)
Multi-Link X2 ECG Adapter and Direct Connect Lead Wire System
| Applicant | Carefusion 303, Inc., Vernon Hills IL, US |
| Decision | Substantially Equivalent, Jun 22, 2017 |
| Received | Nov 23, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K163316
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.