510(k) K953221 ยท KHG Whole Blood Hemoglobin Determination
ABBOTT VISION HEMOGLOBIN (MODIFICATION)
| Applicant | Abbott Laboratories, Abbott Park IL, US |
| Decision | Substantially Equivalent, Sep 29, 1995 |
| Received | Jun 19, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953221
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.