510(k) K851293 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
IMPLANTOFIX
| Applicant | Burron Medical Products, Inc., Bethlehem PA, US |
| Decision | Substantially Equivalent, Jan 9, 1986 |
| Received | Apr 1, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K851293
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.