510(k) K832756 ยท LKY Device, External Penile Rigidity
PRI A PUS
| Applicant | Trans Texas Medical Devices Corp., San Antonio TX, US |
| Decision | Substantially Equivalent, Nov 28, 1983 |
| Received | Aug 16, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832756
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.