510(k) K992199 ยท JBD System, Analysis, Electrophoretic Hemoglobin
ACID HEMOGLOBIN KIT
| Applicant | Helena Laboratories, Beaumont TX, US |
| Decision | Substantially Equivalent, Sep 21, 1999 |
| Received | Jun 30, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992199
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.