510(k) K971768 ยท LKY Device, External Penile Rigidity
RELIANT CHARGER
| Applicant | Walling Medical Equipment Co., Mckinney TX, US |
| Decision | Substantially Equivalent, Sep 29, 1997 |
| Received | May 13, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971768
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.