510(k) K090138 ยท KMI Monitor, Bed Patient
MOBILECARE MONITOR, MODEL 2100
| Applicant | Aframe Digital, Inc., Mosely VA, US |
| Decision | Substantially Equivalent, Apr 24, 2009 |
| Received | Jan 21, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090138
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.