510(k) K870708 ยท LFR Glucose Dehydrogenase, Glucose
GLUCOSCOT II BLOOD GLUCOSE TEST SYSTEM
| Applicant | Kyoto Daiichi Kagaku Co., Ltd., Kyoto, 601, JP |
| Decision | Substantially Equivalent, Feb 2, 1988 |
| Received | Feb 20, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K870708
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.