510(k) K862669 ยท GFD Dermatome
ACTIVATED PARTIAL THROMBOPLASTIN TIME TEST
| Applicant | U. S. Diagnostics, Inc., San Luis Obispo CA, US |
| Decision | Substantially Equivalent, Oct 3, 1986 |
| Received | Jul 14, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862669
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.