510(k) K900803 ยท LFJ Catheter, Subclavian
DUAL LUMEN SUB-CLAVIAN CATHETERS DLSC 600S & 800S
| Applicant | Akcess Medical Products, Inc., New Brunswick NJ, US |
| Decision | Substantially Equivalent, Apr 25, 1990 |
| Received | Feb 20, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900803
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.