510(k) K905080 ยท LFJ Catheter, Subclavian
MED-WEST DUAL LUMEN INTERNAL JUGULAR CATHETER
| Applicant | Kendall Healthcare Products Co. Div.Of Tyco Health, Mansfield MA, US |
| Decision | Substantially Equivalent, Jan 31, 1991 |
| Received | Nov 13, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K905080
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.