510(k) K042379 ยท KHG Whole Blood Hemoglobin Determination
ANEMIAPRO SELF-SCREENER
| Applicant | Biosafe Laboratories, Inc., Lake Forest IL, US |
| Decision | Substantially Equivalent, Dec 15, 2004 |
| Received | Sep 1, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K042379
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.