510(k) K934939 ยท MAJ Catheter, Percutaneous, Intraspinal, Short Term
TEMPORARY SCREENING LEAD/ CATHETER KIT
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, May 24, 1995 |
| Received | Oct 18, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K934939
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.