510(k) K844445 ยท LKY Device, External Penile Rigidity
REVIVE SYSTEM
| Applicant | Revive Systems Corp., Washington DC, US |
| Decision | Substantially Equivalent, Sep 17, 1985 |
| Received | Nov 16, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K844445
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.