510(k) K924568 ยท KMK Device, Intravascular Catheter Securement
TUBE, LEAD, AND CORD HOLDER NO. 102
| Applicant | Ansley Medical Products, Inc., Dallas TX, US |
| Decision | Substantially Equivalent, Nov 23, 1992 |
| Received | Sep 9, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924568
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.