510(k) K020801 ยท JHI Visual, Pregnancy Hcg, Prescription Use
QUICKVUE ONE-STEP HCG-COMBO
| Applicant | Quidel Corp., San Diego CA, US |
| Decision | Substantially Equivalent, May 17, 2002 |
| Received | Mar 12, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020801
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.