510(k) K843699 ยท LHD Device, Fertility Diagnostic, Proceptive
BIOSELF TM 110
| Applicant | Bioself, Inc., Saint-Lambert, Que. Canad, US |
| Decision | Substantially Equivalent, Dec 4, 1984 |
| Received | Sep 20, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K843699
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.