510(k) K053571 ยท JBD System, Analysis, Electrophoretic Hemoglobin
MICROGEL ALKALINE HEMOGLOBIN ELECTROPHORESIS TEST SYSTEM, MICROGEL ACID HEMOGLOBIN ELECTROPHORESIS TEST SYSTEM
| Applicant | Interlab S.R.L., East Stroudsburg PA, US |
| Decision | Substantially Equivalent, Jun 30, 2006 |
| Received | Dec 22, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K053571
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.