510(k) K020258 ยท LKY Device, External Penile Rigidity
SUPPORT SLEEVE
| Applicant | Pos-T-Vac, Inc., Dodge City KS, US |
| Decision | Substantially Equivalent, Apr 4, 2002 |
| Received | Jan 25, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020258
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.