510(k) K945385 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
VITALMAX 800 PLUS/VITALMAX 810 PLUS/MINIPACK 300
| Applicant | Pace Tech, Inc., Clearwater FL, US |
| Decision | Substantially Equivalent, Jan 31, 1995 |
| Received | Nov 3, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K945385
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.