510(k) K063372 ยท DQX Wire, Guide, Catheter
RADIFOCUS GLIDEWIRE ADVANTAGE
| Applicant | Terumo Medical Corp., Elkton MD, US |
| Decision | Substantially Equivalent, Jan 19, 2007 |
| Received | Nov 8, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K063372
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.