510(k) K963988 ยท KRA Catheter, Continuous Flush
INTRAVASCULAR INFUSION DEVICE
| Applicant | Boston Scientific Corp, Natick, MA, US |
| Decision | Substantially Equivalent, Dec 12, 1996 |
| Received | Oct 4, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963988
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.