510(k) K912211 ยท KMK Device, Intravascular Catheter Securement
INTRAVASCULAR CATHETER SECURMENT DEVICE
| Applicant | Inman Liebelt Corp., Arlington TX, US |
| Decision | Substantially Equivalent, Aug 9, 1991 |
| Received | May 20, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912211
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.