510(k) K172394 ยท DRA Catheter, Steerable
Steerable Guide Catheter
| Applicant | Abbott Vascular, Santa Clara CA, US |
| Decision | Substantially Equivalent, Sep 6, 2017 |
| Received | Aug 8, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K172394
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.