510(k) K061539 ยท HFX Clamp, Circumcision
GOMCO CIRCUMCISION CLAMP, MOGEN CLAMP, PLASTIBELL CIRCUMCISION DEVICE
| Applicant | Clinical Innovations, LLC, Murray UT, US |
| Decision | Substantially Equivalent, Sep 20, 2007 |
| Received | Jun 5, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061539
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.