510(k) K925931 ยท LIL Monitor, Penile Tumescence
RT2 RIGIDITY AND TUMESCENCE TEST
| Applicant | Compass Medical Technologies, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Dec 21, 1992 |
| Received | Nov 23, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K925931
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.