Last synced on 9 May 2025 at 11:05 pm

Philips IntelliSite Pathology Solution

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192259
510(k) Type
Special
Applicant
Philips Electronics Nederland B.V.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
9/20/2019
Days to Decision
30 days
Submission Type
Summary

Philips IntelliSite Pathology Solution

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192259
510(k) Type
Special
Applicant
Philips Electronics Nederland B.V.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
9/20/2019
Days to Decision
30 days
Submission Type
Summary