510(k) K802046 ยท BZQ Monitor, Breathing Frequency
PDS MODEL 3000 ADULT RESPIRATION MODULE
| Applicant | General Electric Co., Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 16, 1980 |
| Received | Aug 25, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802046
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.