510(k) K160669 ยท GEH Unit, Cryosurgical, Accessories
ClariFix Device
| Applicant | Arrinex, Inc., Redwood City CA, US |
| Decision | Substantially Equivalent, Jun 24, 2016 |
| Received | Mar 9, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160669
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.