510(k) K930218 ยท MAJ Catheter, Percutaneous, Intraspinal, Short Term
SUBCUTANEOUS TUNNELING NEEDLE AND HANDLES
| Applicant | Concord/Portex, Keene NH, US |
| Decision | Substantially Equivalent, Jul 27, 1993 |
| Received | Jan 15, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930218
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.