510(k) K823312 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
CADIO-RESPIRATORY MONITOR #CR-2
| Applicant | Electromed Intl., Ltd., Walker MI, US |
| Decision | Substantially Equivalent, Nov 30, 1982 |
| Received | Nov 5, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823312
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.