510(k) K881008 ยท LKY Device, External Penile Rigidity
MAXERECT
| Applicant | Kenneth Chapman, Bellaire TX, US |
| Decision | Substantially Equivalent, Oct 12, 1988 |
| Received | Mar 9, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881008
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.