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.. Device class: 2.

Clearance details

Applicant
Hmd Biomedical, Inc.
Product code
Code LFR
Device class
Class 2
Regulation
21 CFR 862.1345
Advisory panel
Clinical Chemistry
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Hsinchu County, TW
Download summary PDFView on FDA.gov ↗

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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, through . 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.