510(k) K802205 ยท BZQ Monitor, Breathing Frequency
ECG/RESPIRATION STIMULATOR
| Applicant | Healthdyne, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Oct 3, 1980 |
| Received | Sep 11, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802205
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.