510(k) K072516 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
MIDMARK DIAGNOSTICS IQMARK VITAL SIGNS MONITOR
| Applicant | Midmark Diagnostics Group, Torrance CA, US |
| Decision | Substantially Equivalent, Oct 18, 2007 |
| Received | Sep 7, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072516
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.