510(k) K800726 ยท KMK Device, Intravascular Catheter Securement
EYEWI ANKORS
| Applicant | Eyevi & Co., Mchenry IL, US |
| Decision | Substantially Equivalent, May 8, 1980 |
| Received | Apr 1, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800726
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.