510(k) K112239 ยท DRA Catheter, Steerable
STEERABLE GUIDE CATHETER
| Applicant | Abbott Vascular, Menlo Park CA, US |
| Decision | Substantially Equivalent, Aug 31, 2011 |
| Received | Aug 4, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K112239
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.