510(k) K881695 ยท LFJ Catheter, Subclavian
DESERET SUBCLAVIAN HEMODIALYSIS CATHETER
| Applicant | Deseret Medical, Inc., Sandy UT, US |
| Decision | Substantially Equivalent, Jun 23, 1988 |
| Received | Apr 19, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881695
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.