510(k) K100811 ยท OBH Monitor, Extracellular Fluid, Lymphedema, Extremity
IMPEDIMED - EXTRACELLULAR FLUID ANALYZER MODEL: L-DEX U400
| Applicant | ImpediMed Limited, San Diego CA, US |
| Decision | Substantially Equivalent, Nov 4, 2011 |
| Received | Mar 22, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100811
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.