510(k) K896750 ยท KOD Catheter, Urological
LOFRIC(R), LOFRIC(R) CATH-KIT
| Applicant | Astra Meditec AB, Sweden, SE |
| Decision | Substantially Equivalent, Aug 6, 1990 |
| Received | Nov 30, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896750
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.