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Atrauman® Ag

Page Type
Cleared 510(K)
510(k) Number
K242758
510(k) Type
Traditional
Applicant
Hartmann USA, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/2024
Days to Decision
88 days
Submission Type
Summary

Atrauman® Ag

Page Type
Cleared 510(K)
510(k) Number
K242758
510(k) Type
Traditional
Applicant
Hartmann USA, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/2024
Days to Decision
88 days
Submission Type
Summary