510(k) K832300 ยท KMK Device, Intravascular Catheter Securement
I.V. FILTER HOLDER
| Applicant | Saxnor Corp., Walker MI, US |
| Decision | Substantially Equivalent, Oct 4, 1983 |
| Received | Jul 13, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832300
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.