510(k) K830282 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
ELECTRONIC EXERCISE #313-PULSE RATE
| Applicant | Walton Manufacturer Co., Walker MI, US |
| Decision | Substantially Equivalent, Apr 14, 1983 |
| Received | Jan 26, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830282
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.