510(k) K843882 ยท KMK Device, Intravascular Catheter Securement
TRENDS LANCET
| Applicant | Orange Medical Instruments, Inc., Costa Mesa CA, US |
| Decision | Substantially Equivalent, Nov 5, 1984 |
| Received | Oct 2, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K843882
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.