510(k) K993343 ยท LKY Device, External Penile Rigidity
ERECXEL ADJUSTABLE PENILE BANDS, CONTREX ADJUSTABLE PENILE BANDS
| Applicant | Erecxel Enterprises, Los Angeles CA, US |
| Decision | Substantially Equivalent, Mar 20, 2000 |
| Received | Oct 5, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K993343
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.