510(k) K831365 ยท LKS Device, Parasite Concentration
TESTCORP ANA
| Applicant | Catheter Technology Corp., Walker MI, US |
| Decision | Substantially Equivalent, Jun 2, 1983 |
| Received | Apr 26, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831365
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.