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Koios DS for Breast

Page Type
Cleared 510(K)
510(k) Number
K190442
510(k) Type
Traditional
Applicant
Koios Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/3/2019
Days to Decision
128 days
Submission Type
Summary

Koios DS for Breast

Page Type
Cleared 510(K)
510(k) Number
K190442
510(k) Type
Traditional
Applicant
Koios Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/3/2019
Days to Decision
128 days
Submission Type
Summary