510(k) K880505 ยท DSI Detector And Alarm, Arrhythmia
ECG/RESPIRATION/ARRHYTHMIA MODULE FOR RM-301
| Applicant | Ppg Industries, Inc., Pleasantville NY, US |
| Decision | Substantially Equivalent, Dec 27, 1988 |
| Received | Feb 5, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880505
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.