510(k) K122688 ยท LFR Glucose Dehydrogenase, Glucose
NOVA MAX MINI BLOOD GLUCOSE AND B-KETONE MONITOR
| Applicant | Nova Biomedical Corporation, Walham MA, US |
| Decision | Substantially Equivalent, Apr 4, 2013 |
| Received | Sep 4, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122688
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.