510(k) K802913 ยท DGC Ige, Antigen, Antiserum, Control
TAN DEM* - IGE KIT
| Applicant | Hybritech, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, May 29, 1981 |
| Received | Nov 18, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802913
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.