510(k) K830917 ยท FAE Prosthesis, Penile
SURGITEK SIZER FOR PENILE PROSTHESIS
| Applicant | Medical Engineering Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 12, 1983 |
| Received | Mar 22, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830917
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.