510(k) K901738 ยท KOD Catheter, Urological
SELFCATH
| Applicant | Vitaid, Ltd., Lewiston NY, US |
| Decision | Substantially Equivalent, Jun 27, 1990 |
| Received | Apr 17, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901738
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.