510(k) K862641 ยท KHG Whole Blood Hemoglobin Determination
U.S. DIAGNOSTIC INC. HEMOGLOBIN TEST (DRY PACK)
| Applicant | U. S. Diagnostics, Inc., San Luis Obispo CA, US |
| Decision | Substantially Equivalent, Aug 21, 1986 |
| Received | Jul 11, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862641
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.