510(k) K071712 ยท DEG Lactoferrin, Antigen, Antiserum, Control
LEUKO EZ VUE
| Applicant | Techlab Inc., Corporate Research Center, Blacksburg VA, US |
| Decision | Substantially Equivalent, Dec 4, 2007 |
| Received | Jun 22, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071712
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.