Last synced on 14 November 2025 at 11:06 pm

Koios DS

Page Type
Cleared 510(K)
510(k) Number
K242130
510(k) Type
Traditional
Applicant
Koios Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/15/2024
Days to Decision
116 days
Submission Type
Summary

Koios DS

Page Type
Cleared 510(K)
510(k) Number
K242130
510(k) Type
Traditional
Applicant
Koios Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/15/2024
Days to Decision
116 days
Submission Type
Summary