Philips IntelliSite Pathology Solution 5.1— 510(k) K242848

Substantially Equivalent

Philips Medical Systems Nederland B.V.

FDA 510(k) clearance K242848 for Philips IntelliSite Pathology Solution 5.1, Substantially Equivalent on 2024-12-10. 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: 2024-09-20
Decision date: 2024-12-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Best, NL

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