510(k) K760120 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
PULSE CARDULE (MODEL 1859/1860 ECG)
| Applicant | Spacelabs, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 20, 1976 |
| Received | Jun 28, 1976 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K760120
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.