510(k) K831845 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
PER-Q-CATH TRAY
| Applicant | Gesco Intl., Inc., Walker MI, US |
| Decision | Substantially Equivalent, Aug 24, 1983 |
| Received | Jun 8, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831845
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.