510(k) K133335 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
POWERPORT IMPLANTABLE PORT
| Applicant | C.R. Bard, Inc., Salt Lake Ciy, UT, US |
| Decision | Substantially Equivalent, Feb 14, 2014 |
| Received | Oct 29, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133335
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.