K113307 is an FDA 510(k) clearance for the GL GOODLIFE SERIES BLOOD GLUCOSE MONITORING SYSMTEM. This device is classified as a Glucose Dehydrogenase, Glucose (Class II - Special Controls, product code LFR).
Submitted by Hmd Biomedical, Inc. (Hsinchu County, TW). The FDA issued a Cleared decision on July 27, 2012, 262 days after receiving the submission on November 8, 2011.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1345.
| 510(k) Number | K113307 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | November 08, 2011 |
| Decision Date | July 27, 2012 |
| Days to Decision | 262 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | Summary PDF |
| Product Code | LFR — Glucose Dehydrogenase, Glucose |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.1345 |