510(k) K103695 ยท HFX Clamp, Circumcision
PREPEX SYSTEM
| Applicant | Circ Medtech, Chalotte NC, US |
| Decision | Substantially Equivalent, Jan 10, 2012 |
| Received | Dec 17, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K103695
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.