FDA 510(k) Applications Submitted by Donna Peled

FDA 510(k) Number Submission Date Device Name Applicant
K241871 06/27/2024 Philips IntelliSite Pathology Solution Philips Medical Systems Nederland B.V.
K242848 09/20/2024 Philips IntelliSite Pathology Solution 5.1 Philips Medical Systems Nederland B.V.
K243871 12/17/2024 Philips IntelliSite Pathology Solution 5.1 Philips Medical Systems Nederland B.V.


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