510(k) K202375 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
ZOLL Propaq M
| Applicant | ZOLL Medical Corporation, Chelsmford MA, US |
| Decision | Substantially Equivalent, Mar 9, 2021 |
| Received | Aug 20, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202375
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.