510(k) K163261 ยท FZP Clip, Implantable
AtriClip PRO, PRO2, and PRO V LAA Exclusion System devices with preloaded Gillinov-Cosgrove Clip
| Applicant | AtriCure, Inc., Mason OH, US |
| Decision | Substantially Equivalent, May 19, 2017 |
| Received | Nov 21, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K163261
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.