510(k) K081527 ยท GQL Antisera, Fluorescent, Herpesvirus Hominis 1,2
LIGHT DIAGNOSTICS HSV 1/2 TYPING DFA KIT
| Applicant | Millipore Corporation, Temecula CA, US |
| Decision | Substantially Equivalent, Apr 1, 2009 |
| Received | Jun 2, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081527
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.