510(k) K833848 ยท LFJ Catheter, Subclavian
DUAL LUMEN SUBCLAVIAN CANNULA
| Applicant | Shiley, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 8, 1983 |
| Received | Nov 4, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833848
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.