510(k) K890402 ยท FAE Prosthesis, Penile
MENTOR CYLINDER PROTECTOR TOOL (INFLATABLE PENILE)
| Applicant | Mentor Corp., Goleta CA, US |
| Decision | Substantially Equivalent, Aug 3, 1989 |
| Received | Jan 24, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890402
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.