510(k) K932397 ยท LKY Device, External Penile Rigidity
RELIANT
| Applicant | Allan Walling Medical Equipment Co., Dallas TX, US |
| Decision | Substantially Equivalent, Mar 7, 1994 |
| Received | May 18, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932397
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.