510(k) K183687 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
LifeWindow LW8 Lite
| Applicant | Digicare Biomedical Technology, Inc., Boynton Beach FL, US |
| Decision | Substantially Equivalent, Sep 25, 2019 |
| Received | Dec 28, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183687
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.