510(k) K963106 ยท GGP Test, Qualitative And Quantitative Factor Deficiency
CHROMOLIZE PAI-1 KIT
| Applicant | Medical Diagnostic Technologies, Inc., Ventura CA, US |
| Decision | Substantially Equivalent, Nov 18, 1996 |
| Received | Aug 12, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963106
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.