510(k) K812461 ยท JHI Visual, Pregnancy Hcg, Prescription Use
TANDEM QUALITATIVE HCG KIT
| Applicant | Hybritech, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 13, 1981 |
| Received | Aug 31, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K812461
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.