510(k) K780484 ยท FIQ Cannula, A-V Shunt
SILASTIC BRAND PENILE IMPLANT
| Applicant | Dow Corning Corp. Healthcare Industries Materials, Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 17, 1978 |
| Received | Mar 27, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780484
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.