510(k) K162432 ยท DSA Cable, Transducer And Electrode, Patient, (Including Connector)
Multi-Link X2 ECG Cable and Lead Wire System
| Applicant | Carefusion 2200, Inc., Vernon Hills IL, US |
| Decision | Substantially Equivalent, Jan 18, 2017 |
| Received | Aug 31, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162432
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.