510(k) K912316 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter
QUIKPAC-II ONE STEP PREGNANCY HOME TEST
| Applicant | Syntron Bioresearch, Inc., Vista CA, US |
| Decision | Substantially Equivalent, Jul 24, 1991 |
| Received | May 24, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912316
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.