510(k) K190273 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
T3 Platform software
| Applicant | Etiometry, Inc., Boston MA, US |
| Decision | Substantially Equivalent, Dec 8, 2019 |
| Received | Feb 8, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190273
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.