510(k) K994073 ยท KHG Whole Blood Hemoglobin Determination
HEMOSITE TEST SYSTEM
| Applicant | Gds Technology, LLC, Elkhart IN, US |
| Decision | Substantially Equivalent, Jan 14, 2000 |
| Received | Dec 2, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K994073
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.