510(k) K892887 ยท FIQ Cannula, A-V Shunt
ST SERIES SAF-T-SHUNTS ARTERIOVENOUS CANNULA
| Applicant | Akcess Medical Products, Inc., New Brunswick NJ, US |
| Decision | Substantially Equivalent, May 15, 1989 |
| Received | Apr 20, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K892887
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.