510(k) K851646 ยท LIL Monitor, Penile Tumescence
VIBRECTOR
| Applicant | Multicept, Aps., Copenhagen, DK |
| Decision | Substantially Equivalent, Aug 21, 1985 |
| Received | Apr 19, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K851646
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.