510(k) K992442 ยท LKY Device, External Penile Rigidity
V.T.S., INC. (V.T.-3)
| Applicant | Vts, Inc., Newkirk OK, US |
| Decision | Substantially Equivalent, Oct 5, 1999 |
| Received | Jul 22, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992442
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.