510(k) K160956 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
LD-Oxi system
| Applicant | Ld Technology, LLC, Miami FL, US |
| Decision | Substantially Equivalent, Jul 6, 2016 |
| Received | Apr 5, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K160956
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.