510(k) K102211 ยท DQX Wire, Guide, Catheter
CRUISER 18 GUIDEWIRE
| Applicant | Brivant, Ltd., Galway, IE |
| Decision | Substantially Equivalent, Sep 3, 2010 |
| Received | Aug 5, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K102211
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.