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Genteel Lancing Device

Page Type
Cleared 510(K)
510(k) Number
K153670
510(k) Type
Traditional
Applicant
Genteel, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/12/2016
Days to Decision
143 days
Submission Type
Summary

Genteel Lancing Device

Page Type
Cleared 510(K)
510(k) Number
K153670
510(k) Type
Traditional
Applicant
Genteel, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/12/2016
Days to Decision
143 days
Submission Type
Summary