Last synced on 14 November 2025 at 11:06 pm

Dayspring Lite

Page Type
Cleared 510(K)
510(k) Number
K212287
510(k) Type
Special
Applicant
Koya Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/2021
Days to Decision
62 days
Submission Type
Summary

Dayspring Lite

Page Type
Cleared 510(K)
510(k) Number
K212287
510(k) Type
Special
Applicant
Koya Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/2021
Days to Decision
62 days
Submission Type
Summary