510(k) K063429 ยท HFX Clamp, Circumcision
GMD UNIVERSAL CIRCUMCISION CLAMP, MODEL 200
| Applicant | Generic Medical Device, Inc., Houston TX, US |
| Decision | Substantially Equivalent, Jan 17, 2007 |
| Received | Nov 13, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K063429
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.