510(k) K841202 ยท LIL Monitor, Penile Tumescence
DACOMED RIGISCAN SYSTEM
| Applicant | Dacomed Corp., Walker MI, US |
| Decision | Substantially Equivalent, Jul 6, 1984 |
| Received | Mar 21, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K841202
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.