510(k) K053111 ยท GFO Activated Partial Thromboplastin
STA-CEPHASCREEN KIT
| Applicant | Diagnostica Stago, Inc., Parisppany NJ, US |
| Decision | Substantially Equivalent, May 4, 2006 |
| Received | Nov 4, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K053111
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.