510(k) K895871 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
LIFEPORT POLYURETHANE CATHETER
| Applicant | Strato Medical Corp., Beverly MA, US |
| Decision | Substantially Equivalent, Nov 17, 1989 |
| Received | Oct 4, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895871
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.