510(k) K964300 ยท DBI Complement C4, Antigen, Antiserum, Control
N-ASSAY TIA MULTI V-NL
| Applicant | Crestat Diagnostics, Inc., Murrieta CA, US |
| Decision | Substantially Equivalent, Jul 14, 1997 |
| Received | Oct 29, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964300
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.