510(k) K130056 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
PATIENT MONITOR
| Applicant | Ld Technology, LLC, Miami FL, US |
| Decision | Substantially Equivalent, Apr 11, 2013 |
| Received | Jan 9, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130056
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.