510(k) K950436 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
WITT BIOMEDICAL SERIES IV
| Applicant | Witt Biomedical Corporation, Melbourne FL, US |
| Decision | Substantially Equivalent, Nov 2, 1995 |
| Received | Feb 2, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950436
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.