510(k) K781885 ยท CDW Diacetyl-Monoxime, Urea Nitrogen
SERUM, BLOOD UREA NITIOGEN
| Applicant | Fisher Scientific Co., LLC, Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 20, 1978 |
| Received | Nov 7, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781885
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.