Philips IntelliSite Pathology Solution— 510(k) K241871

Substantially Equivalent

Philips Medical Systems Nederland B.V.

FDA 510(k) clearance K241871 for Philips IntelliSite Pathology Solution, Substantially Equivalent on 2024-12-02. 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: 2024-06-27
Decision date: 2024-12-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Best, NL

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