510(k) K823197 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
MODEL 8300 TESTER
| Applicant | Medicon, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Dec 30, 1982 |
| Received | Oct 26, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823197
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.