510(k) K182565 ยท GXH Device, Surgical, Cryogenic
AtriCure cryoICE cryoSPHERE cryoablation probe
| Applicant | AtriCure, Inc., Mason OH, US |
| Decision | Substantially Equivalent, Nov 9, 2018 |
| Received | Sep 18, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K182565
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.