510(k) K880498 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
RM-301 PATIENT MONITOR
| Applicant | Ppg Industries, Inc., Pleasantville NY, US |
| Decision | Substantially Equivalent, May 13, 1988 |
| Received | Feb 5, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880498
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.