510(k) K945134 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
PORTABLE PATIENT MONITOR
| Applicant | Hewlett-Packard Co., Andover MA, US |
| Decision | Substantially Equivalent, Oct 28, 1994 |
| Received | Oct 20, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K945134
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.