510(k) K921014 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
MODEL M2350A AND M2360A WAVEVUE CENTRAL MONITOR
| Applicant | Hewlett-Packard Co., Waltham MA, US |
| Decision | Substantially Equivalent, Oct 1, 1992 |
| Received | Mar 3, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K921014
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.