510(k) K991532 ยท DHA System, Test, Human Chorionic Gonadotropin
DRX QT. HCG
| Applicant | Metrika, Inc., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Sep 17, 1999 |
| Received | May 3, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991532
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.