510(k) K862108 ยท DHA System, Test, Human Chorionic Gonadotropin
ENZYMUN-TEST HCG
| Applicant | Boehringer Mannheim Corp., Indianapolis IN, US |
| Decision | Substantially Equivalent, Aug 19, 1986 |
| Received | Jun 3, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862108
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.