510(k) K860698 ยท LKY Device, External Penile Rigidity
THE BOOSTER
| Applicant | Knapps Corp., Newark CA, US |
| Decision | Substantially Equivalent, Feb 3, 1989 |
| Received | Feb 25, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860698
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.