510(k) K900559 ยท LKY Device, External Penile Rigidity
RESPONSE EXTERNAL PENILE RIGIDITY DEVICE
| Applicant | Smith-Collins Pharmaceutical, Inc., West Chester PA, US |
| Decision | Substantially Equivalent, May 2, 1990 |
| Received | Feb 7, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900559
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.