510(k) K954093 ยท FEN Device, Cystometric, Hydraulic
LUMAX (MODIFICATION)
| Applicant | Medamicus, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Jan 11, 1996 |
| Received | Aug 9, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954093
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.