510(k) K904406 ยท LKY Device, External Penile Rigidity
EER ERECTION ENHANCED RESPONDER
| Applicant | Eer, Inc., Mechanicsburg PA, US |
| Decision | Substantially Equivalent, Feb 25, 1991 |
| Received | Sep 24, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904406
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.