510(k) K882232 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter
DISCOVER(R)
| Applicant | Carter Products, Cranbury NJ, US |
| Decision | Substantially Equivalent, Oct 25, 1988 |
| Received | May 27, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882232
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.