510(k) K202062 ยท PHZ Abnormal Breath Sound Device
wheezo WheezeRate Detector
| Applicant | Respiri Limited, Melbourne, AU |
| Decision | Substantially Equivalent, Mar 11, 2021 |
| Received | Jul 27, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202062
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.