510(k) K122435 ยท LFR Glucose Dehydrogenase, Glucose
NOVA ONE BLOOD GLUCOSE MONITOR
| Applicant | Nova Biomedical Corporation, Walham MA, US |
| Decision | Substantially Equivalent, Dec 20, 2012 |
| Received | Aug 10, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122435
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.