510(k) K863302 ยท KOD Catheter, Urological
MODIFIED FOLEY CATHETER
| Applicant | Sheridan Catheter Corp., Argyle NY, US |
| Decision | Substantially Equivalent, Oct 3, 1986 |
| Received | Aug 25, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863302
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.