510(k) K101299 ยท LFR Glucose Dehydrogenase, Glucose
ACCU-CHEK AVIVA PLUS BLOOD GLUCOSE MONITORING SYSTEM
| Applicant | Roche Diagnostics, Indianapolis IN, US |
| Decision | Substantially Equivalent, Sep 21, 2011 |
| Received | May 10, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101299
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.