510(k) K033583 ยท DQO Catheter, Intravascular, Diagnostic
PROGREAT
| Applicant | Terumo Medical Corp., Elkton MD, US |
| Decision | Substantially Equivalent, Dec 12, 2003 |
| Received | Nov 13, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K033583
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.