510(k) K920409 ยท LKY Device, External Penile Rigidity
DACOMED BATTERY OPERATED VACUUM ERECTION DEVICE
| Applicant | Dacomed Corp., Minneapolis MN, US |
| Decision | Substantially Equivalent, May 11, 1992 |
| Received | Jan 31, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920409
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.