510(k) K990008 ยท LKY Device, External Penile Rigidity
ERCO-RIBBON -C
| Applicant | Ercons, Inc., New York NY, US |
| Decision | Substantially Equivalent, Feb 24, 1999 |
| Received | Jan 4, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990008
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.