510(k) K800519 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
HEARTWATCH
| Applicant | D. Jenkins, Walker MI, US |
| Decision | Substantially Equivalent, Sep 26, 1980 |
| Received | Mar 6, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800519
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.