510(k) K862412 ยท LLD Port & Catheter, Implanted, Subcutaneous, Intraperitoneal
INTESTOPLANT
| Applicant | Burron Medical Products, Inc., Bethlehem PA, US |
| Decision | Substantially Equivalent, Nov 13, 1986 |
| Received | Jun 25, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862412
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.