510(k) K910622 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
GESCO PER-Q-CATH REPAIR KIT
| Applicant | Gesco Intl., Inc., San Antonio TX, US |
| Decision | Unknown, Mar 29, 1991 |
| Received | Feb 12, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910622
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.