510(k) K822099 ยท LIL Monitor, Penile Tumescence
BIOREM 2000
| Applicant | Biorem, Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 27, 1982 |
| Received | Jul 16, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K822099
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.