510(k) K832121 ยท LIL Monitor, Penile Tumescence
DACOMED SNAP-GAUGE
| Applicant | Dacomed Corp. MD, US |
| Decision | Substantially Equivalent, Jul 18, 1983 |
| Received | Jun 30, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832121
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.