510(k) K924369 ยท KMK Device, Intravascular Catheter Securement
ILS(TM) - INVASIVE LINE SEPARATOR
| Applicant | 2-Rn Corp., Melbourne FL, US |
| Decision | Substantially Equivalent, Feb 5, 1993 |
| Received | Aug 28, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924369
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.