510(k) K072141 ยท CEO Phosphomolybdate (Colorimetric), Inorganic Phosphorus
S40 CLINICAL ANALYZER, S TEST IP, S TEST UA
| 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 K072141
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.