510(k) K162608 ยท GEH Unit, Cryosurgical, Accessories
ClariFix Device
| Applicant | Arrinex, Inc., Redwood City CA, US |
| Decision | Substantially Equivalent, Feb 14, 2017 |
| Received | Sep 19, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162608
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.