510(k) K090040 ยท DQO Catheter, Intravascular, Diagnostic
RADIFOCUS GLIDECATH (OR RADIFOCUS GLIDECATH XP)
| Applicant | Terumo Medical Corp., Elkton MD, US |
| Decision | Substantially Equivalent, Feb 6, 2009 |
| Received | Jan 6, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090040
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.