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Aperio AT2 DX System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190332
510(k) Type
Traditional
Applicant
Leica Biosystems Imaging, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/20/2019
Days to Decision
95 days
Submission Type
Summary

Aperio AT2 DX System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190332
510(k) Type
Traditional
Applicant
Leica Biosystems Imaging, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/20/2019
Days to Decision
95 days
Submission Type
Summary