510(k) K964538 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
R-PORT STANDARD IMPLANTABLE VASCULAR ACCESS SYSTEM
| Applicant | Boston Scientific Corp, Natick, MA, US |
| Decision | Substantially Equivalent, Mar 10, 1997 |
| Received | Nov 12, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964538
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.