510(k) K122590 ยท DQX Wire, Guide, Catheter
RADIFOCUS GLIDEWIRE ADVANTAGE, RADIFOCUS GLIDEWIRE ADVANTAGE
| Applicant | Terumo Medical Corporation, Somerset NJ, US |
| Decision | Substantially Equivalent, Mar 1, 2013 |
| Received | Aug 24, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K122590
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.