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E1000 Dx Digital Pathology Solution

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241717
510(k) Type
Traditional
Applicant
Shandon Diagnostics Limited
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
2/28/2025
Days to Decision
259 days
Submission Type
Summary

E1000 Dx Digital Pathology Solution

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241717
510(k) Type
Traditional
Applicant
Shandon Diagnostics Limited
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
2/28/2025
Days to Decision
259 days
Submission Type
Summary