510(k) K820637 ยท KOD Catheter, Urological
CATH-HOLD
| Applicant | Womco Products, Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 25, 1982 |
| Received | Mar 8, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820637
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.