510(k) K933624 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
VITALMAX 4000
| Applicant | Pace Tech, Inc., Clearwater FL, US |
| Decision | Substantially Equivalent, Jul 19, 1994 |
| Received | Jul 19, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933624
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.