510(k) K810114 ยท FIQ Cannula, A-V Shunt
VASCULAR ACCESS SYSTEM
| Applicant | Bentley Laboratories, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 26, 1981 |
| Received | Dec 15, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810114
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.