510(k) K861831 ยท KNK Acid, Uric, Uricase (Colorimetric)
REFLOTRON URIC ACID
| Applicant | Boehringer Mannheim Corp., Indianapolis IN, US |
| Decision | Substantially Equivalent, Jul 11, 1986 |
| Received | May 13, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K861831
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.