510(k) K980752 ยท LKY Device, External Penile Rigidity
XTEND
| Applicant | Walling Medical Equipment Co., Mckinney TX, US |
| Decision | Substantially Equivalent, May 6, 1998 |
| Received | Feb 20, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980752
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.