510(k) K922801 ยท GNY Antisera, Fluorescent, Adenovirus 1-33
RESP. PANEL 1 INDIRECT IMMUNOFLUORESCENCE ASSAY
| Applicant | Light Diagnostics, Temecula CA, US |
| Decision | Substantially Equivalent, Jan 6, 1993 |
| Received | Jun 10, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922801
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.