510(k) K883592 ยท LFJ Catheter, Subclavian
IMPRA DUAL LUMEN SUBCLAVIAN - FEMORAL CATHETER
| Applicant | Impra, Inc., Tempe AZ, US |
| Decision | Unknown, Dec 8, 1988 |
| Received | Aug 23, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883592
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.