510(k) K884645 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
PATIENT MONITOR RIGEL MODEL MULTICARE 429
| Applicant | Rigel Medical Electronics, Inc., Mill Valley CA, US |
| Decision | Substantially Equivalent, Feb 2, 1989 |
| Received | Nov 7, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884645
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.