MENTOR NIPPLE RECONSTRUCTION DEVICE
| Applicant | Mentor Corp., Goleta CA, US |
| Decision | Substantially Equivalent, Feb 24, 1987 |
| Received | Jan 7, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K870059
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.