Philips IntelliSite Pathology Solution 5.1— 510(k) K243871

Substantially Equivalent

Philips Medical Systems Nederland B.V.

FDA 510(k) clearance K243871 for Philips IntelliSite Pathology Solution 5.1, Substantially Equivalent on 2025-03-06. Applicant: Philips Medical Systems Nederland B.V..

Clearance details

Applicant: Philips Medical Systems Nederland B.V.
Product code: Code PSY
Advisory panel: Pathology
Date received: 2024-12-17
Decision date: 2025-03-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Best, NL

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