510(k) K823209 ยท LHD Device, Fertility Diagnostic, Proceptive
BIOSELF 101
| Applicant | Bioself, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 15, 1983 |
| Received | Oct 28, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823209
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.