510(k) K093915 ยท FIG Clamp, Tubing, Blood, Automatic
DEKA TAC DEVICE
| Applicant | Deka Research & Development Corp., Manchester NH, US |
| Decision | Substantially Equivalent, Aug 23, 2011 |
| Received | Dec 22, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093915
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.