510(k) K822316 ยท DRI Monitor, Line Isolation
HEART MONITOR BRACELET ALARM
| Applicant | Hmba, Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 21, 1982 |
| Received | Aug 3, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K822316
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.