510(k) K882531 ยท LKY Device, External Penile Rigidity
MODIFIED L.J.'S SEX HELPER
| Applicant | L.J. Fant & Co., Glencoe AL, US |
| Decision | Substantially Equivalent, Dec 8, 1988 |
| Received | Jun 22, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882531
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.