510(k) K003104 ยท LJF Device, Antimicrobial Drug Removal
BACT/ALERT CSR
| Applicant | Organon Teknika Corp., Durham NC, US |
| Decision | Substantially Equivalent, Oct 20, 2000 |
| Received | Aug 29, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K003104
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.