Philips IntelliSite Pathology Solution— 510(k) DEN160056

Unknown

Philips Medical Systems Nederland B.V.

FDA 510(k) clearance DEN160056 for Philips IntelliSite Pathology Solution, Unknown on 2017-04-12. 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: 2016-12-01
Decision date: 2017-04-12
Decision: Unknown
Clearance type: Direct
Location: Best, NL

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