510(k) K971840 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
OMNI-TRAK MODEL 3150 SERIES PATIENT MONITORING SYSTEM
| Applicant | Invivo Research, Inc., Orlando FL, US |
| Decision | Substantially Equivalent, Mar 4, 1998 |
| Received | May 19, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971840
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.