510(k) K823463 ยท LHD Device, Fertility Diagnostic, Proceptive
RIGHT TIME RHYTHM CLOCK
| Applicant | P.K. Morgan Instruments, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 17, 1983 |
| Received | Nov 19, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823463
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.