510(k) K941781 ยท LIL Monitor, Penile Tumescence
RIGISCAN PLUS RIGIDITY ASSESSMENT SYSTEM
| Applicant | Dacomed Corp., Minneapolis MN, US |
| Decision | Substantially Equivalent, Aug 25, 1994 |
| Received | Apr 11, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K941781
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.