510(k) K072215 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
TITANIUM POWERPORT ISP IMPLANTED PORT
| Applicant | C.R. Bard, Inc., Salt Lake Ciy, UT, US |
| Decision | Substantially Equivalent, Nov 1, 2007 |
| Received | Aug 9, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K072215
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.