510(k) K000730 ยท LKY Device, External Penile Rigidity
IMPOAID
| Applicant | Impoaid, Inc., Stillwater MN, US |
| Decision | Substantially Equivalent, Oct 19, 2000 |
| Received | Mar 6, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000730
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.