510(k) K830885 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
GOULD MODEL IM3000-IM3100 BATTERY POWER
| Applicant | Gould, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jun 22, 1983 |
| Received | Mar 21, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830885
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.