510(k) K895101 ยท KHG Whole Blood Hemoglobin Determination
BIOTRACK HEMOGLOBIN TEST CARTRIDGE
| Applicant | Biotrack, Inc., Mountain View CA, US |
| Decision | Substantially Equivalent, Oct 10, 1989 |
| Received | Aug 15, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895101
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.