510(k) K034065 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
MODIFICATION TO X-PORT DUO PORT
| Applicant | C.R. Bard, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Jan 15, 2004 |
| Received | Dec 29, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K034065
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.