510(k) K982888 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
VAXCEL IMPANTABLE VASCULAR ACCESS SYSTEM
| Applicant | Boston Scientific Corp, Natick, MA, US |
| Decision | Substantially Equivalent, Oct 20, 1998 |
| Received | Aug 17, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982888
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.