510(k) K960272 ยท MLD Monitor, St Segment With Alarm
EAGLE 3000/3100 PATIENT MONITOR
| Applicant | Marquette Electronics, Inc., Milwaukee WI, US |
| Decision | Substantially Equivalent, Oct 2, 1996 |
| Received | Jan 18, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960272
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.