510(k) K101674 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
WVSM (WIRELESS VITAL SIGNS MONITOR), MODEL 5.0
| Applicant | Athena Gtx, Des Moines IA, US |
| Decision | Substantially Equivalent, Jul 21, 2010 |
| Received | Jun 15, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101674
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.