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Koios DS

Page Type
Cleared 510(K)
510(k) Number
K212616
510(k) Type
Traditional
Applicant
Koios Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/2021
Days to Decision
120 days
Submission Type
Summary

Koios DS

Page Type
Cleared 510(K)
510(k) Number
K212616
510(k) Type
Traditional
Applicant
Koios Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/2021
Days to Decision
120 days
Submission Type
Summary