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TRUEdraw Lancing Device, Mini Lancing Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221072
510(k) Type
Traditional
Applicant
Trividia Health
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/2022
Days to Decision
189 days
Submission Type
Summary

TRUEdraw Lancing Device, Mini Lancing Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221072
510(k) Type
Traditional
Applicant
Trividia Health
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/2022
Days to Decision
189 days
Submission Type
Summary