Philips IntelliSite Pathology Solution— 510(k) K172174

Substantially Equivalent

Philips Medical Systems Nederland B.V.

FDA 510(k) clearance K172174 for Philips IntelliSite Pathology Solution, Substantially Equivalent on 2017-10-04. 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: 2017-07-19
Decision date: 2017-10-04
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Best, NL

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