510(k) K904486 ยท LKY Device, External Penile Rigidity
SUPPORT PUMP
| Applicant | Numedtec, Inc., Libertyville IL, US |
| Decision | Substantially Equivalent, Dec 14, 1990 |
| Received | Oct 2, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904486
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.