510(k) K031942 ยท MHI Giardia Spp.
XPECT GIARDIA LATERAL FLOW ASSAY, MODEL 2450020
| Applicant | Remel, Inc., Ramsey MN, US |
| Decision | Substantially Equivalent, Nov 18, 2003 |
| Received | Jun 24, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K031942
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.