510(k) K871942 ยท LFJ Catheter, Subclavian
PERM-CATH CATHETER KIT
| Applicant | Quinton, Inc., Bothell WA, US |
| Decision | Substantially Equivalent, Jun 17, 1987 |
| Received | May 19, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K871942
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.