510(k) K973860 ยท NGE Test, Luteinizing Hormone (Lh), Over The Counter
OVULON MONITOR
| Applicant | Conception Technology, Inc., Ft. Collins CO, US |
| Decision | Substantially Equivalent, Jan 7, 1998 |
| Received | Oct 9, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973860
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.