510(k) K931833 ยท DQO Catheter, Intravascular, Diagnostic
MODIFIED LUER
| Applicant | Medi-Dyne, Inc., Glens Falls NY, US |
| Decision | Substantially Equivalent, Sep 28, 1993 |
| Received | Mar 8, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K931833
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.