510(k) K893830 ยท DQO Catheter, Intravascular, Diagnostic
HEMO-ALERT
| Applicant | Koregon Enterprise, Inc., Beaverton OR, US |
| Decision | Substantially Equivalent, Oct 12, 1989 |
| Received | May 24, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893830
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.