510(k) K930197 ยท KMK Device, Intravascular Catheter Securement
KWIK BOARD
| Applicant | Astral, Ltd., San Rafael CA, US |
| Decision | Substantially Equivalent, Apr 20, 1993 |
| Received | Jan 14, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930197
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.