510(k) K875160 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
RIGEL MODEL MULTICARE 409
| Applicant | Rigel Medical Electronics, Inc., Mill Valley CA, US |
| Decision | Substantially Equivalent, Jun 28, 1988 |
| Received | Dec 15, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K875160
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.