510(k) K912152 ยท MHI Giardia Spp.
CELLABS GIARDIA CEL I.F. TEST
| Applicant | Celltech Diagnostics , Ltd., Suite 11oo, Washington DC, US |
| Decision | Substantially Equivalent, Aug 12, 1991 |
| Received | May 15, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912152
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.