510(k) K872249 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
SIRECUST MODEL 960 AND 961 PATIENT MONITORING
| Applicant | Medical Electronics Laboratories, Inc., Danvers MA, US |
| Decision | Substantially Equivalent, Jul 21, 1987 |
| Received | Jun 12, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K872249
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.