510(k) K915215 ยท LFK Catheter, Femoral
CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH. KITS
| Applicant | Akcess Medical Products, Inc., New Brunswick NJ, US |
| Decision | Unknown, Mar 27, 1992 |
| Received | Nov 18, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K915215
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.