510(k) K903199 ยท DQO Catheter, Intravascular, Diagnostic
HOLLOW LUMEN NEEDLE, PART NUMBER: MX920
| Applicant | Medex, Inc., Dublin OH, US |
| Decision | Substantially Equivalent, Dec 17, 1990 |
| Received | Jul 20, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903199
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.