510(k) K882252 ยท CEP Radioimmunoassay, Luteinizing Hormone
PHASE II LH KIT
| Applicant | Vitek Systems, Inc., Rockland MA, US |
| Decision | Substantially Equivalent, Aug 4, 1988 |
| Received | May 31, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882252
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.