510(k) K870165 ยท KOD Catheter, Urological
FOLEY CATHETER
| Applicant | Acorn Medical Products, Palo Alto CA, US |
| Decision | Substantially Equivalent, Apr 17, 1987 |
| Received | Jan 14, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K870165
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.