510(k) K102175 ยท JHI Visual, Pregnancy Hcg, Prescription Use
RAPIDVUE HCG TEST
| Applicant | Quidel Corporation, San Diego CA, US |
| Decision | Substantially Equivalent, Aug 25, 2010 |
| Received | Aug 2, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K102175
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.