Last synced on 23 May 2025 at 11:06 pm

VIDAvision

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K200990
510(k) Type
Traditional
Applicant
VIDA Diagnostics Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/2020
Days to Decision
114 days
Submission Type
Summary

VIDAvision

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K200990
510(k) Type
Traditional
Applicant
VIDA Diagnostics Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/2020
Days to Decision
114 days
Submission Type
Summary