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Aperio GT 450 DX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232202
510(k) Type
Traditional
Applicant
Leica Biosystems Imaging, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/16/2024
Days to Decision
266 days
Submission Type
Summary

Aperio GT 450 DX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232202
510(k) Type
Traditional
Applicant
Leica Biosystems Imaging, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/16/2024
Days to Decision
266 days
Submission Type
Summary