510(k) K881342 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
IMPLANTOFIX II IMPLANTABLE DRUG DELIVERY SYSTEM
| Applicant | Burron Medical, Inc., Bethlehem PA, US |
| Decision | Substantially Equivalent, Aug 9, 1988 |
| Received | Mar 30, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881342
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.