510(k) K072140 ยท CFR Hexokinase, Glucose
S40 CLINICAL ANALYZER, S TEST BIL, S TEST BUN, S TEST GLU
| Applicant | Alfa Wassermann Diagnostic Technologies, Inc., West Caldwell NJ, US |
| Decision | Substantially Equivalent, Jun 24, 2008 |
| Received | Aug 2, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072140
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.