510(k) K130338 ยท OBH Monitor, Extracellular Fluid, Lymphedema, Extremity
IMPEDIMED - BIS EXTRA CELLULAR FLUID ANALYSIS
| Applicant | ImpediMed Limited, Washington DC, US |
| Decision | Substantially Equivalent, May 31, 2013 |
| Received | Feb 11, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130338
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.