510(k) K895942 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
GESCO DUAL LUMEN PER-Q-CATH-DL
| Applicant | Gesco Intl., Inc., San Antonio TX, US |
| Decision | Substantially Equivalent, Jul 2, 1990 |
| Received | Oct 11, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895942
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.