510(k) K912440 ยท CGA Glucose Oxidase, Glucose
ULTRA BLOOD GLUCOSE MONITORING SYSTEM
| Applicant | Home Diagnostics, Inc., Eatontown NJ, US |
| Decision | Substantially Equivalent, Jul 17, 1991 |
| Received | Jun 3, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912440
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.