510(k) K093815 ยท OMG Antisera, Fluorescent, Human Metapneumovirus
LIGHT DIAGNOSTICS HUMAN METAPNEUMOVIRUS DFA KIT, MODEL CATALOG NUMBER 3124
| Applicant | Millipore Corporation, Temecula CA, US |
| Decision | Substantially Equivalent, Mar 12, 2010 |
| Received | Dec 14, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093815
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.