Philips IntelliSite Pathology Solution— 510(k) K203845

Substantially Equivalent

Philips Medical Systems Nederland B.V.

FDA 510(k) clearance K203845 for Philips IntelliSite Pathology Solution, Substantially Equivalent on 2021-09-17. 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: 2020-12-31
Decision date: 2021-09-17
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Best, NL

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