510(k) K880066 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
MODEL 303D AND 403D ADULT HEART RATE & RESPIRATOR
| Applicant | Ivy Biomedical Systems, Inc., Branford CT, US |
| Decision | Substantially Equivalent, Mar 22, 1988 |
| Received | Jan 11, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880066
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.