510(k) K020969 ยท LKY Device, External Penile Rigidity
VACURECT VACUUM CONSTRICTION DEVICE
| Applicant | Vacurect Manufacturing (Pty) , Ltd., North Attleboro MA, US |
| Decision | Substantially Equivalent, Jun 5, 2002 |
| Received | Mar 26, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020969
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.