510(k) K884096 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
PATIENT MONITOR MODEL 701
| Applicant | Ivy Biomedical Systems, Inc., Branford CT, US |
| Decision | Substantially Equivalent, Feb 23, 1989 |
| Received | Sep 28, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884096
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.