510(k) K930225 ยท KMK Device, Intravascular Catheter Securement
K-LOK CATHETER SECUREMENT DEVICE
| Applicant | K-Lok, Inc., Boca Raton FL, US |
| Decision | Substantially Equivalent, Apr 21, 1993 |
| Received | Jan 15, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930225
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.