510(k) K151095 ยท HFX Clamp, Circumcision
Circumplast Circumcision Device
| Applicant | Novadien Healthcare, Mount Lewis, AU |
| Decision | Substantially Equivalent, Sep 18, 2015 |
| Received | Apr 23, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151095
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.