510(k) K823135 ยท LFJ Catheter, Subclavian
DOUBLE LUMEN SUBCLAVIAN CATHETER
| Applicant | Abbott Laboratories, Abbott Park IL, US |
| Decision | Substantially Equivalent, Mar 7, 1983 |
| Received | Oct 28, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823135
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.