510(k) K924180 ยท KMK Device, Intravascular Catheter Securement
I.V. PRO
| Applicant | I.V. - Pro Tek, Inc., Seabrook TX, US |
| Decision | Substantially Equivalent, Mar 16, 1993 |
| Received | Aug 19, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924180
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.