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QScout Lab; QScout RLD

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230878
510(k) Type
Traditional
Applicant
Ad Astra Diagnostics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/2023
Days to Decision
229 days
Submission Type
Summary

QScout Lab; QScout RLD

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230878
510(k) Type
Traditional
Applicant
Ad Astra Diagnostics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/2023
Days to Decision
229 days
Submission Type
Summary