510(k) K910501 ยท LFJ Catheter, Subclavian
PERMANENT SILICONE CATHETERS
| Applicant | Akcess Medical Products, Inc., New Brunswick NJ, US |
| Decision | Substantially Equivalent, Apr 29, 1991 |
| Received | Feb 5, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910501
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.