510(k) K822134 ยท LFJ Catheter, Subclavian
SHIELY DUEL LUMEN SUBCLAVIAN CANNULA
| Applicant | Shiley, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Aug 3, 1982 |
| Received | Jul 20, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K822134
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.