510(k) K900370 ยท HFX Clamp, Circumcision
ONE/CIRC (CIRCUMCISION CLAMP)
| Applicant | Bionix Development Corp., Toledo OH, US |
| Decision | Substantially Equivalent, Apr 16, 1990 |
| Received | Jan 25, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900370
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.