510(k) K864190 ยท KMK Device, Intravascular Catheter Securement
E-Z HOLD - #4060
| Applicant | John F. Greer Co., Inc., Oakland CA, US |
| Decision | Substantially Equivalent, Jan 14, 1987 |
| Received | Oct 27, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K864190
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.