510(k) K142203 ยท GXH Device, Surgical, Cryogenic
Atricure Cryo Module System; cryoICE cryoablation probe
| Applicant | AtriCure, Inc., West Chester OH, US |
| Decision | Substantially Equivalent, Nov 25, 2014 |
| Received | Aug 11, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142203
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.