510(k) K832543 ยท LKY Device, External Penile Rigidity
MALE THERAPEUTIC POTENT AID
| Applicant | Mace'S Scientific, Virginia Beach VA, US |
| Decision | Substantially Equivalent, Dec 27, 1983 |
| Received | Jul 29, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832543
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.