510(k) K891753 ยท LFJ Catheter, Subclavian
DUAL LUMEN SUB-CLAVIAN CATHETER, DLSC 600 & 800
| Applicant | Akcess Medical Products, Inc., New Brunswick NJ, US |
| Decision | Substantially Equivalent, Jun 8, 1989 |
| Received | Mar 23, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K891753
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.