GL GOODLIFE SERIES BLOOD GLUCOSE MONITORING SYSMTEM— 510(k) K113307

Substantially Equivalent

Hmd Biomedical, Inc.

FDA 510(k) clearance K113307 for GL GOODLIFE SERIES BLOOD GLUCOSE MONITORING SYSMTEM, Substantially Equivalent on 2012-07-27. Applicant: Hmd Biomedical, Inc..

Clearance details

Applicant: Hmd Biomedical, Inc.
Product code: Code LFR
Advisory panel: Clinical Chemistry
Date received: 2011-11-08
Decision date: 2012-07-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hsinchu County, TW

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Adverse events under product code LFR

product code LFR

Death: 3
Malfunction: 1,634
Total: 1,637

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.