510(k) K971582 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
NIPRO CORELESS NEEDLE/CORELESS NEEDLE SET
| Applicant | Nipro Medical Corp., Lexington KY, US |
| Decision | Substantially Equivalent, Dec 22, 1997 |
| Received | Apr 30, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971582
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.