510(k) K945551 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
CELSITE(TM) DUAL VENOUS SYSTEM
| Applicant | B. Braun of America, Inc., Bethlehem PA, US |
| Decision | Substantially Equivalent, Apr 21, 1995 |
| Received | Nov 14, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K945551
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.