510(k) K891611 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
MODELS 6526,6527,6528 PERCU. TRANS. ANGIO. CATH.
| Applicant | Medtronic Versaflex, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Jun 12, 1989 |
| Received | Mar 20, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K891611
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.