510(k) K904140 ยท LFJ Catheter, Subclavian
SINGLE LUMEN CATHETERS, MODIFICATION
| Applicant | Akcess Medical Products, Inc., New Brunswick NJ, US |
| Decision | Substantially Equivalent, Nov 27, 1990 |
| Received | Sep 6, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904140
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.