510(k) K892666 ยท FIQ Cannula, A-V Shunt
SAF-T-SHUNT, S-300 SERIES
| Applicant | Akcess Medical Products, Inc., New Brunswick NJ, US |
| Decision | Substantially Equivalent, May 4, 1989 |
| Received | Apr 13, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K892666
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.