510(k) K031898 ยท GKR System, Hemoglobin, Automated
EKF DIAGNOSTIC HEMO CONTROL HEMOGLOBIN MEASUREMENT SYSTEM
| Applicant | Ekf Diagnostic GmbH, Egale WI, US |
| Decision | Substantially Equivalent, Sep 24, 2003 |
| Received | Jun 19, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K031898
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.