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RIGHTEST Lancing Device GD500, GE Lancing Device, iGlucose Lancing Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221062
510(k) Type
Traditional
Applicant
Bionime Corporation
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
9/26/2022
Days to Decision
168 days
Submission Type
Summary

RIGHTEST Lancing Device GD500, GE Lancing Device, iGlucose Lancing Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221062
510(k) Type
Traditional
Applicant
Bionime Corporation
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
9/26/2022
Days to Decision
168 days
Submission Type
Summary