510(k) K830372 ยท LJF Device, Antimicrobial Drug Removal
ARTIMICROBIAL REMOVAL DEVICE
| Applicant | Marion Laboratories, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Apr 8, 1983 |
| Received | Feb 4, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830372
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.