510(k) K003839 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
CENTRAL VENOUS CATHETER
| Applicant | Boston Scientific Corp, Natick, MA, US |
| Decision | Substantially Equivalent, Aug 1, 2001 |
| Received | Dec 12, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K003839
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.