510(k) K881290 ยท LFJ Catheter, Subclavian
MODIFIED SHILEY DUAL LUMEN SUBCLAVIAN CANNULA
| Applicant | Shiley, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Apr 27, 1988 |
| Received | Mar 28, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881290
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.