510(k) K153359 · LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
BardPort®, SlimPort®, and X-Port® Implanted Ports
| Applicant | C.R. Bard, Inc., Salt Lake Ciy, UT, US |
| Decision | Substantially Equivalent, May 20, 2016 |
| Received | Nov 20, 2015 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K153359
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.