510(k) K923117 ยท DXT Injector And Syringe, Angiographic
CAVERNOSOMETRY MODULE FOR MENUET
| Applicant | Dantec Medical, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Feb 22, 1993 |
| Received | Jun 26, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923117
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.