510(k) K945061 ยท KOD Catheter, Urological
NOPROFILE OLBERT CATHETER SYSTEM
| Applicant | Meadox Surgimed, Inc., Oakland NJ, US |
| Decision | Substantially Equivalent, Mar 9, 1995 |
| Received | Oct 14, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K945061
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.