510(k) K991479 ยท LIL Monitor, Penile Tumescence
VISER PENILE TUMESCENCE MONITOR
| Applicant | Laborie Medical Tech Corp., Williston VT, US |
| Decision | Substantially Equivalent, Jul 7, 1999 |
| Received | Apr 28, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991479
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.