510(k) K896060 ยท LKY Device, External Penile Rigidity
ERECTION INDUCER DEVICE (EID)
| Applicant | Performance Medical, Inc., Great Neck NY, US |
| Decision | Substantially Equivalent, Mar 20, 1990 |
| Received | Oct 18, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896060
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.