510(k) K896357 ยท LKY Device, External Penile Rigidity
SAFE AID DEVICE IMPOTENCE DEVICE
| Applicant | Dr. John P. March, Sacramento CA, US |
| Decision | Substantially Equivalent, Apr 25, 1990 |
| Received | Nov 6, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896357
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.