510(k) K880664 ยท DSI Detector And Alarm, Arrhythmia
MORTARA INSTRUMENT MODEL ELI-XR (TREADMILL INCLUDED)
| Applicant | Mortara Instrument, Inc., Milwaukee WI, US |
| Decision | Substantially Equivalent, Mar 9, 1988 |
| Received | Feb 18, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880664
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.