510(k) K911796 ยท DHA System, Test, Human Chorionic Gonadotropin
IMMULITE(TM) HCG
| Applicant | Cirrus Diagnostics, Inc., Chester NJ, US |
| Decision | Substantially Equivalent, Jun 20, 1991 |
| Received | Apr 22, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911796
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.