510(k) K900371 ยท FAE Prosthesis, Penile
MENTOR MODIFIED MALLEABLE PENILE PROSTHESES
| Applicant | Mentor Corp., Goleta CA, US |
| Decision | Substantially Equivalent, Nov 2, 1990 |
| Received | Jan 26, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900371
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.