Last synced on 30 November 2024 at 11:09 am

Koios DS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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