510(k) K202306 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
T3 Platform software
| Applicant | Etiometry, Inc., Boston MA, US |
| Decision | Substantially Equivalent, Nov 25, 2020 |
| Received | Aug 14, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202306
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.