510(k) K872843 ยท JLP Spectrophotometric Method, Pregnanediol
OVEIA (TM) DUAL ANALYTE
| Applicant | Boots-Celltech Diagnostics, Inc., Berkshire, England, GB |
| Decision | Substantially Equivalent, Feb 2, 1988 |
| Received | Jul 20, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K872843
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.