510(k) K140329 ยท KRA Catheter, Continuous Flush
RENEGADE HI-FLO MICROCATHETER, MICROCATHETER KIT, FATHOM SYSTEM, FATHOM KIT
| Applicant | Boston Scientific, Maple Grove MN, US |
| Decision | Substantially Equivalent, May 15, 2014 |
| Received | Feb 10, 2014 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K140329
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.