510(k) K960342 ยท LKY Device, External Penile Rigidity
POS-T-VAC AVP-1000 & MVP-700
| Applicant | Pos-T-Vac, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Mar 1, 1996 |
| Received | Jan 24, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960342
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.