510(k) K960855 ยท CGA Glucose Oxidase, Glucose
PRESTIGE BLOOD GLUCOSE MONITORING SYSTEM,METER,TEST STRIPS & PRESTIGE HIGH AND LOW GLUCOSE CONTROL
| Applicant | Home Diagnostics, Inc., Ft Lauderdale FL, US |
| Decision | Substantially Equivalent, Nov 7, 1996 |
| Received | Mar 1, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960855
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.