510(k) K020714 ยท GBM Catheter, Urethral
RUSCH FLONEIL; FLOCATH INTROGEL
| Applicant | Rusch Intl., Jeffrey NH, US |
| Decision | Substantially Equivalent, Jul 1, 2002 |
| Received | Mar 5, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020714
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.