510(k) K962489 ยท GGP Test, Qualitative And Quantitative Factor Deficiency
CHROMOLIZE TPA ASSAY KIT
| Applicant | Medical Diagnostic Technologies, Inc., Ventura CA, US |
| Decision | Substantially Equivalent, Jul 31, 1996 |
| Received | Jun 26, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962489
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.